Compositions and methods for the therapy and diagnosis of lung cancer

ABSTRACT

Compositions and methods for the therapy and diagnosis of cancer, particularly lung cancer, are disclosed. Illustrative compositions comprise one or more lung tumor polypeptides, immunogenic portions thereof, polynucleotides that encode such polypeptides, antigen presenting cell that expresses such polypeptides, and T cells that are specific for cells expressing such polypeptides. The disclosed compositions are useful, for example, in the diagnosis, prevention and/or treatment of diseases, particularly lung cancer.

CROSS REFERENCE TO RELATED APPLICATIONS

[0001] The present application is related to U.S. patent application Ser. Nos. 09/735,705, filed Dec. 12, 2000; 09/685,696, filed Oct. 9, 2000; 09/662,786, filed Sep. 15, 2000; 09/643,597, filed Aug. 21, 2000; 09/630,940 filed Aug. 2, 2000; 09/606,421 filed Jun. 28, 2000; 09/542,615 filed Apr. 4, 2000; 09/510,376 filed Feb. 22, 2000; 09/480,884 filed Jan. 10, 2000; 09/476,496 filed Dec. 30, 1999; 09/466,396 filed Dec. 17, 1999; 09/285,479 filed Apr. 2, 1999; 09/221,107 filed Dec. 22, 1998; 09/123,912 filed Jul. 27, 1998; 09/040,802 filed Mar. 18, 1998; each a CIP of the previous application and pending, and all incorporated by reference herein.

TECHNICAL FIELD OF THE INVENTION

[0002] The present invention relates generally to therapy and diagnosis of cancer, such as lung cancer. The invention is more specifically related to polypeptides, comprising at least a portion of a lung tumor protein, and to polynucleotides encoding such polypeptides. Such polypeptides and polynucleotides are useful in pharmaceutical compositions, e.g., vaccines, and other compositions for the diagnosis and treatment of lung cancer.

BACKGROUND OF THE INVENTION

[0003] Lung cancer is the primary cause of cancer death among both men and women in the U.S., with an estimated 172,000 new cases being reported in 1994. The five-year survival rate among all lung cancer patients, regardless of the stage of disease at diagnosis, is only 13%. This contrasts with a five-year survival rate of 46% among cases detected while the disease is still localized. However, only 16% of lung cancers are discovered before the disease has spread.

[0004] Early detection is difficult since clinical symptoms are often not seen until the disease has reached an advanced stage. Currently, diagnosis is aided by the use of chest x-rays, analysis of the type of cells contained in sputum and fiberoptic examination of the bronchial passages. Treatment regimens are determined by the type and stage of the cancer, and include surgery, radiation therapy and/or chemotherapy. In spite of considerable research into therapies for the disease, lung cancer remains difficult to treat.

[0005] Accordingly, there remains a need in the art for improved vaccines, treatment methods and diagnostic techniques for lung cancer.

SUMMARY OF THE INVENTION

[0006] In one aspect, the present invention provides polynucleotide compositions comprising a sequence selected from the group consisting of:

[0007] (a) sequences provided in SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434;

[0008] (b) complements of the sequences provided in SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434;

[0009] (c) sequences consisting of at least 20 contiguous residues of a sequence provided in SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434;

[0010] (d) sequences that hybridize to a sequence provided in SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434, under moderately stringent conditions;

[0011] (e) sequences having at least 75% identity to a sequence of SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434;

[0012] (f) sequences having at least 90% identity to a sequence of SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434; and

[0013] (g) degenerate variants of a sequence provided in SEQ ID NO: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434.

[0014] In one preferred embodiment, the polynucleotide compositions of the invention are expressed in at least about 20%, more preferably in at least about 30%, and most preferably in at least about 50% of lung tumors samples tested, at a level that is at least about 2-fold, preferably at least about 5-fold, and most preferably at least about 10-fold higher than that for normal tissues.

[0015] The present invention, in another aspect, provides polypeptide compositions comprising an amino acid sequence that is encoded by a polynucleotide sequence described above. In certain specific embodiments, such polypeptide compositions comprise an amino acid sequence selected from the group consisting of sequences recited in SEQ ID NO: 152, 155, 156, 165, 166, 169, 170, 172, 174, 176, 226-252, 338-344, 346, 350, 357, 361, 363, 365, 367, 369, 376-382, 387-419, 423, 427, 430 and 433.

[0016] In certain preferred embodiments, the polypeptides and/or polynucleotides of the present invention are immunogenic, i.e., they are capable of eliciting an immune response, particularly a humoral and/or cellular immune response, as further described herein.

[0017] The present invention further provides fragments, variants and/or derivatives of the disclosed polypeptide and/or polynucleotide sequences, wherein the fragments, variants and/or derivatives preferably have a level of immunogenic activity of at least about 50%, preferably at least about 70% and more preferably at least about 90% of the level of immunogenic activity of a polypeptide sequence set forth in SEQ ID NOs: 152, 155, 156, 165, 166, 169, 170, 172, 174, 176, 226-252, 338-344, 346, 350, 357, 361, 363, 365, 367, 369, 376-382, 387-419, 423, 427, 430 and 433, or a polypeptide sequence encoded by a polynucleotide sequence set forth in SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434.

[0018] The present invention further provides polynucleotides that encode a polypeptide described above, expression vectors comprising such polynucleotides and host cells transformed or transfected with such expression vectors.

[0019] Within other aspects, the present invention provides pharmaceutical compositions comprising a polypeptide or polynucleotide as described above and a physiologically acceptable carrier.

[0020] Within a related aspect of the present invention, the pharmaceutical compositions, e.g., vaccine compositions, are provided for prophylactic or therapeutic applications. Such compositions generally comprise an immunogenic polypeptide or polynucleotide of the invention and an immunostimulant, such as an adjuvant.

[0021] The present invention further provides pharmaceutical compositions that comprise: (a) an antibody or antigen-binding fragment thereof that specifically binds to a polypeptide of the present invention, or a fragment thereof, and (b) a physiologically acceptable carrier.

[0022] Within further aspects, the present invention provides pharmaceutical compositions comprising: (a) an antigen presenting cell that expresses a polypeptide as described above and (b) a pharmaceutically acceptable carrier or excipient. Illustrative antigen presenting cells include dendritic cells, macrophages, monocytes, fibroblasts and B cells.

[0023] Within related aspects, pharmaceutical compositions are provided that comprise: (a) an antigen presenting cell that expresses a polypeptide as described above and (b) an immunostimulant.

[0024] The present invention further provides, in other aspects, fusion proteins that comprise at least one polypeptide as described above, as well as polynucleotides encoding such fusion proteins, typically in the form of pharmaceutical compositions, e.g., vaccine compositions, comprising a physiologically acceptable carrier and/or an immunostimulant. The fusions proteins may comprise multiple immunogenic polypeptides or portions/variants thereof, as described herein, and may further comprise one or more polypeptide segments for facilitating the expression, purification and/or immunogenicity of the polypeptide(s).

[0025] Within further aspects, the present invention provides methods for stimulating an immune response in a patient, preferably a T cell response in a human patient, comprising administering a pharmaceutical composition described herein. The patient may be afflicted with lung cancer, in which case the methods provide treatment for the disease, or patient considered at risk for such a disease may be treated prophylactically.

[0026] Within further aspects, the present invention provides methods for inhibiting the development of a cancer in a patient, comprising administering to a patient a pharmaceutical composition as recited above. The patient may be afflicted with lung cancer, in which case the methods provide treatment for the disease, or patient considered at risk for such a disease may be treated prophylactically.

[0027] The present invention further provides, within other aspects, methods for removing tumor cells from a biological sample, comprising contacting a biological sample with T cells that specifically react with a polypeptide of the present invention, wherein the step of contacting is performed under conditions and for a time sufficient to permit the removal of cells expressing the protein from the sample.

[0028] Within related aspects, methods are provided for inhibiting the development of a cancer in a patient, comprising administering to a patient a biological sample treated as described above.

[0029] Methods are further provided, within other aspects, for stimulating and/or expanding T cells specific for a polypeptide of the present invention, comprising contacting T cells with one or more of: (i) a polypeptide as described above; (ii) a polynucleotide encoding such a polypeptide; and/or (iii) an antigen presenting cell that expresses such a polypeptide; under conditions and for a time sufficient to permit the stimulation and/or expansion of T cells. Isolated T cell populations comprising T cells prepared as described above are also provided.

[0030] Within further aspects, the present invention provides methods for inhibiting the development of a cancer in a patient, comprising administering to a patient an effective amount of a T cell population as described above.

[0031] The present invention further provides methods for inhibiting the development of a cancer in a patient, comprising the steps of: (a) incubating CD4⁺ and/or CD8⁺ T cells isolated from a patient with one or more of: (i) a polypeptide comprising at least an immunogenic portion of polypeptide disclosed herein; (ii) a polynucleotide encoding such a polypeptide; and (iii) an antigen-presenting cell that expressed such a polypeptide; and (b) administering to the patient an effective amount of the proliferated T cells, and thereby inhibiting the development of a cancer in the patient. Proliferated cells may, but need not, be cloned prior to administration to the patient.

[0032] Within further aspects, the present invention provides methods for determining the presence or absence of a cancer, preferably a lung cancer, in a patient comprising: (a) contacting a biological sample obtained from a patient with a binding agent that binds to a polypeptide as recited above; (b) detecting in the sample an amount of polypeptide that binds to the binding agent; and (c) comparing the amount of polypeptide with a predetermined cut-off value, and therefrom determining the presence or absence of a cancer in the patient. Within preferred embodiments, the binding agent is an antibody, more preferably a monoclonal antibody.

[0033] The present invention also provides, within other aspects, methods for monitoring the progression of a cancer in a patient. Such methods comprise the steps of: (a) contacting a biological sample obtained from a patient at a first point in time with a binding agent that binds to a polypeptide as recited above; (b) detecting in the sample an amount of polypeptide that binds to the binding agent; (c) repeating steps (a) and (b) using a biological sample obtained from the patient at a subsequent point in time; and (d) comparing the amount of polypeptide detected in step (c) with the amount detected in step (b) and therefrom monitoring the progression of the cancer in the patient.

[0034] The present invention further provides, within other aspects, methods for determining the presence or absence of a cancer in a patient, comprising the steps of: (a) contacting a biological sample obtained from a patient with an oligonucleotide that hybridizes to a polynucleotide that encodes a polypeptide of the present invention; (b) detecting in the sample a level of a polynucleotide, preferably mRNA, that hybridizes to the oligonucleotide; and (c) comparing the level of polynucleotide that hybridizes to the oligonucleotide with a predetermined cut-off value, and therefrom determining the presence or absence of a cancer in the patient. Within certain embodiments, the amount of mRNA is detected via polymerase chain reaction using, for example, at least one oligonucleotide primer that hybridizes to a polynucleotide encoding a polypeptide as recited above, or a complement of such a polynucleotide. Within other embodiments, the amount of mRNA is detected using a hybridization technique, employing an oligonucleotide probe that hybridizes to a polynucleotide that encodes a polypeptide as recited above, or a complement of such a polynucleotide.

[0035] In related aspects, methods are provided for monitoring the progression of a cancer in a patient, comprising the steps of: (a) contacting a biological sample obtained from a patient with an oligonucleotide that hybridizes to a polynucleotide that encodes a polypeptide of the present invention; (b) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide; (c) repeating steps (a) and (b) using a biological sample obtained from the patient at a subsequent point in time; and (d) comparing the amount of polynucleotide detected in step (c) with the amount detected in step (b) and therefrom monitoring the progression of the cancer in the patient.

[0036] Within further aspects, the present invention provides antibodies, such as monoclonal antibodies, that bind to a polypeptide as described above, as well as diagnostic kits comprising such antibodies. Diagnostic kits comprising one or more oligonucleotide probes or primers as described above are also provided.

[0037] These and other aspects of the present invention will become apparent upon reference to the following detailed description and attached drawings. All references disclosed herein are hereby incorporated by reference in their entirety as if each was incorporated individually.

BRIEF DESCRIPTION OF THE DRAWINGS AND SEQUENCE IDENTIFIERS

[0038] SEQ ID NO: 1 is the determined cDNA sequence for LST-S1-2

[0039] SEQ ID NO: 2 is the determined cDNA sequence for LST-S1-28

[0040] SEQ ID NO: 3 is the determined cDNA sequence for LST-S1-90

[0041] SEQ ID NO: 4 is the determined cDNA sequence for LST-S1-144

[0042] SEQ ID NO: 5 is the determined cDNA sequence for LST-S1-133

[0043] SEQ ID NO: 6 is the determined cDNA sequence for LST-S1-169

[0044] SEQ ID NO: 7 is the determined cDNA sequence for LST-S2-6

[0045] SEQ ID NO: 8 is the determined cDNA sequence for LST-S2-11

[0046] SEQ ID NO: 9 is the determined cDNA sequence for LST-S2-17

[0047] SEQ ID NO: 10 is the determined cDNA sequence for LST-S2-25

[0048] SEQ ID NO: 11 is the determined cDNA sequence for LST-S2-39

[0049] SEQ ID NO: 12 is a first determined cDNA sequence for LST-S2-43

[0050] SEQ ID NO: 13 is a second determined cDNA sequence for LST-S2-43

[0051] SEQ ID NO: 14 is the determined cDNA sequence for LST-S2-65

[0052] SEQ ID NO: 15 is the determined cDNA sequence for LST-S2-68

[0053] SEQ ID NO: 16 is the determined cDNA sequence for LST-S2-72

[0054] SEQ ID NO: 17 is the determined cDNA sequence for LST-S2-74

[0055] SEQ ID NO: 18 is the determined cDNA sequence for LST-S2-103

[0056] SEQ ID NO: 19 is the determined cDNA sequence for LST-S2-N1-1F

[0057] SEQ ID NO: 20 is the determined cDNA sequence for LST-S2-N1-2A

[0058] SEQ ID NO: 21 is the determined cDNA sequence for LST-S2-N1-4H

[0059] SEQ ID NO: 22 is the determined cDNA sequence for LST-S2-N1-5A

[0060] SEQ ID NO: 23 is the determined cDNA sequence for LST-S2-N1-6B

[0061] SEQ ID NO: 24 is the determined cDNA sequence for LST-S2-N1-7B

[0062] SEQ ID NO: 25 is the determined cDNA sequence for LST-S2-N1-7H

[0063] SEQ ID NO: 26 is the determined cDNA sequence for LST-S2-N1-8A

[0064] SEQ ID NO: 27 is the determined cDNA sequence for LST-S2-N1-8D

[0065] SEQ ID NO: 28 is the determined cDNA sequence for LST-S2-N1-9A

[0066] SEQ ID NO: 29 is the determined cDNA sequence for LST-S2-N1-9E

[0067] SEQ ID NO: 30 is the determined cDNA sequence for LST-S2-N1-10A

[0068] SEQ ID NO: 31 is the determined cDNA sequence for LST-S2-N1-10G

[0069] SEQ ID NO: 32 is the determined cDNA sequence for LST-S2-N1-11A

[0070] SEQ ID NO: 33 is the determined cDNA sequence for LST-S2-N1-12C

[0071] SEQ ID NO: 34 is the determined cDNA sequence for LST-S2-N1-12E

[0072] SEQ ID NO: 35 is the determined cDNA sequence for LST-S2-B1-3D

[0073] SEQ ID NO: 36 is the determined cDNA sequence for LST-S2-B1-6C

[0074] SEQ ID NO: 37 is the determined cDNA sequence for LST-S2-B1-5D

[0075] SEQ ID NO: 38 is the determined cDNA sequence for LST-S2-B1-5F

[0076] SEQ ID NO: 39 is the determined cDNA sequence for LST-S2-B1-6G

[0077] SEQ ID NO: 40 is the determined cDNA sequence for LST-S2-B1-8A

[0078] SEQ ID NO: 41 is the determined cDNA sequence for LST-S2-B1-8D

[0079] SEQ ID NO: 42 is the determined cDNA sequence for LST-S2-B1-10A

[0080] SEQ ID NO: 43 is the determined cDNA sequence for LST-S2-B1-9B

[0081] SEQ ID NO: 44 is the determined cDNA sequence for LST-S2-B1-9F

[0082] SEQ ID NO: 45 is the determined cDNA sequence for LST-S2-B1-12D

[0083] SEQ ID NO: 46 is the determined cDNA sequence for LST-S2-I2-2B

[0084] SEQ ID NO: 47 is the determined cDNA sequence for LST-S2-I2-5F

[0085] SEQ ID NO: 48 is the determined cDNA sequence for LST-S2-I2-6B

[0086] SEQ ID NO: 49 is the determined cDNA sequence for LST-S2-I2-7F

[0087] SEQ ID NO: 50 is the determined cDNA sequence for LST-S2-I2-8G

[0088] SEQ ID NO: 51 is the determined cDNA sequence for LST-S2-I2-9E

[0089] SEQ ID NO: 52 is the determined cDNA sequence for LST-S2-I2-12B

[0090] SEQ ID NO: 53 is the determined cDNA sequence for LST-S2-H2-2C

[0091] SEQ ID NO: 54 is the determined cDNA sequence for LST-S2-H2-1G

[0092] SEQ ID NO: 55 is the determined cDNA sequence for LST-S2-H2-4G

[0093] SEQ ID NO: 56 is the determined cDNA sequence for LST-S2-H2-3H

[0094] SEQ ID NO: 57 is the determined cDNA sequence for LST-S2-H2-5G

[0095] SEQ ID NO: 58 is the determined cDNA sequence for LST-S2-H2-9B

[0096] SEQ ID NO: 59 is the determined cDNA sequence for LST-S2-H2-10H

[0097] SEQ ID NO: 60 is the determined cDNA sequence for LST-S2-H2-12D

[0098] SEQ ID NO: 61 is the determined cDNA sequence for LST-S3-2

[0099] SEQ ID NO: 62 is the determined cDNA sequence for LST-S3-4

[0100] SEQ ID NO: 63 is the determined cDNA sequence for LST-S3-7

[0101] SEQ ID NO: 64 is the determined cDNA sequence for LST-S3-8

[0102] SEQ ID NO: 65 is the determined cDNA sequence for LST-S3-12

[0103] SEQ ID NO: 66 is the determined cDNA sequence for LST-S3-13

[0104] SEQ ID NO: 67 is the determined cDNA sequence for LST-S3-14

[0105] SEQ ID NO: 68 is the determined cDNA sequence for LST-S3-16

[0106] SEQ ID NO: 69 is the determined cDNA sequence for LST-S3-21

[0107] SEQ ID NO: 70 is the determined cDNA sequence for LST-S3-22

[0108] SEQ ID NO: 71 is the determined cDNA sequence for LST-S1-7

[0109] SEQ ID NO: 72 is the determined cDNA sequence for LST-S1-A-1E

[0110] SEQ ID NO: 73 is the determined cDNA sequence for LST-S1-A-1G

[0111] SEQ ID NO: 74 is the determined cDNA sequence for LST-S1-A-3E

[0112] SEQ ID NO: 75 is the determined cDNA sequence for LST-S1-A-4E

[0113] SEQ ID NO: 76 is the determined cDNA sequence for LST-S1-A-6D

[0114] SEQ ID NO: 77 is the determined cDNA sequence for LST-S1-A-8D

[0115] SEQ ID NO: 78 is the determined cDNA sequence for LST-S1-A-10A

[0116] SEQ ID NO: 79 is the determined cDNA sequence for LST-S1-A-10C

[0117] SEQ ID NO: 80 is the determined cDNA sequence for LST-S1-A-9D

[0118] SEQ ID NO: 81 is the determined cDNA sequence for LST-S1-A-10D

[0119] SEQ ID NO: 82 is the determined cDNA sequence for LST-S1-A-9H

[0120] SEQ ID NO: 83 is the determined cDNA sequence for LST-S1-A-11D

[0121] SEQ ID NO: 84 is the determined cDNA sequence for LST-S1-A-12D

[0122] SEQ ID NO: 85 is the determined cDNA sequence for LST-S1-A-11E

[0123] SEQ ID NO: 86 is the determined cDNA sequence for LST-S1-A-12E

[0124] SEQ ID NO: 87 is the determined cDNA sequence for L513S (T3).

[0125] SEQ ID NO: 88 is the determined cDNA sequence for L513S contig 1.

[0126] SEQ ID NO: 89 is a first determined cDNA sequence for L514S.

[0127] SEQ ID NO: 90 is a second determined cDNA sequence for L514S.

[0128] SEQ ID NO: 91 is a first determined cDNA sequence for L516S.

[0129] SEQ ID NO: 92 is a second determined cDNA sequence for L516S.

[0130] SEQ ID NO: 93 is the determined cDNA sequence for L517S.

[0131] SEQ ID NO: 94 is the extended cDNA sequence for LST-S1-169 (also known as L519S).

[0132] SEQ ID NO: 95 is a first determined cDNA sequence for L520S.

[0133] SEQ ID NO: 96 is a second determined cDNA sequence for L520S.

[0134] SEQ ID NO: 97 is a first determined cDNA sequence for L521S.

[0135] SEQ ID NO: 98 is a second determined cDNA sequence for L521S.

[0136] SEQ ID NO: 99 is the determined cDNA sequence for L522S.

[0137] SEQ ID NO: 100 is the determined cDNA sequence for L523S.

[0138] SEQ ID NO: 101 is the determined cDNA sequence for L524S.

[0139] SEQ ID NO: 102 is the determined cDNA sequence for L525S.

[0140] SEQ ID NO: 103 is the determined cDNA sequence for L526S.

[0141] SEQ ID NO: 104 is the determined cDNA sequence for L527S.

[0142] SEQ ID NO: 105 is the determined cDNA sequence for L528S.

[0143] SEQ ID NO: 106 is the determined cDNA sequence for L529S.

[0144] SEQ ID NO: 107 is a first determined cDNA sequence for L530S.

[0145] SEQ ID NO: 108 is a second determined cDNA sequence for L530S.

[0146] SEQ ID NO: 109 is the determined full-length cDNA sequence for L531S short form

[0147] SEQ ID NO: 110 is the amino acid sequence encoded by SEQ ID NO: 109.

[0148] SEQ ID NO: 111 is the determined full-length cDNA sequence for L531S long form

[0149] SEQ ID NO: 112 is the amino acid sequence encoded by SEQ ID NO: 111.

[0150] SEQ ID NO: 113 is the determined full-length cDNA sequence for L520S.

[0151] SEQ ID NO: 114 is the amino acid sequence encoded by SEQ ID NO: 113.

[0152] SEQ ID NO: 115 is the determined cDNA sequence for contig 1.

[0153] SEQ ID NO: 116 is the determined cDNA sequence for contig 3.

[0154] SEQ ID NO: 117 is the determined cDNA sequence for contig 4.

[0155] SEQ ID NO: 118 is the determined cDNA sequence for contig 5.

[0156] SEQ ID NO: 119 is the determined cDNA sequence for contig 7.

[0157] SEQ ID NO: 120 is the determined cDNA sequence for contig 8.

[0158] SEQ ID NO: 121 is the determined cDNA sequence for contig 9.

[0159] SEQ ID NO: 122 is the determined cDNA sequence for contig 10.

[0160] SEQ ID NO: 123 is the determined cDNA sequence for contig 12.

[0161] SEQ ID NO: 124 is the determined cDNA sequence for contig 11.

[0162] SEQ ID NO: 125 is the determined cDNA sequence for contig 13 (also known as L761P).

[0163] SEQ ID NO: 126 is the determined cDNA sequence for contig 15.

[0164] SEQ ID NO: 127 is the determined cDNA sequence for contig 16.

[0165] SEQ ID NO: 128 is the determined cDNA sequence for contig 17.

[0166] SEQ ID NO: 129 is the determined cDNA sequence for contig 19.

[0167] SEQ ID NO: 130 is the determined cDNA sequence for contig 20.

[0168] SEQ ID NO: 131 is the determined cDNA sequence for contig 22.

[0169] SEQ ID NO: 132 is the determined cDNA sequence for contig 24.

[0170] SEQ ID NO: 133 is the determined cDNA sequence for contig 29.

[0171] SEQ ID NO: 134 is the determined cDNA sequence for contig 31.

[0172] SEQ ID NO: 135 is the determined cDNA sequence for contig 33.

[0173] SEQ ID NO: 136 is the determined cDNA sequence for contig 38.

[0174] SEQ ID NO: 137 is the determined cDNA sequence for contig 39.

[0175] SEQ ID NO: 138 is the determined cDNA sequence for contig 41.

[0176] SEQ ID NO: 139 is the determined cDNA sequence for contig 43.

[0177] SEQ ID NO: 140 is the determined cDNA sequence for contig 44.

[0178] SEQ ID NO: 141 is the determined cDNA sequence for contig 45.

[0179] SEQ ID NO: 142 is the determined cDNA sequence for contig 47.

[0180] SEQ ID NO: 143 is the determined cDNA sequence for contig 48.

[0181] SEQ ID NO: 144 is the determined cDNA sequence for contig 49.

[0182] SEQ ID NO: 145 is the determined cDNA sequence for contig 50.

[0183] SEQ ID NO: 146 is the determined cDNA sequence for contig 53.

[0184] SEQ ID NO: 147 is the determined cDNA sequence for contig 54.

[0185] SEQ ID NO: 148 is the determined cDNA sequence for contig 56.

[0186] SEQ ID NO: 149 is the determined cDNA sequence for contig 57.

[0187] SEQ ID NO: 150 is the determined cDNA sequence for contig 58.

[0188] SEQ ID NO: 151 is the full-length cDNA sequence for L530S.

[0189] SEQ ID NO: 152 is the amino acid sequence encoded by SEQ ID NO: 151

[0190] SEQ ID NO: 153 is the full-length cDNA sequence of a first variant of L514S

[0191] SEQ ID NO: 154 is the full-length cDNA sequence of a second variant of L514S

[0192] SEQ ID NO: 155 is the amino acid sequence encoded by SEQ ID NO: 153.

[0193] SEQ ID NO: 156 is the amino acid sequence encoded by SEQ ID NO: 154.

[0194] SEQ ID NO: 157 is the determined cDNA sequence for contig 59.

[0195] SEQ ID NO: 158 is the full-length cDNA sequence for L763P (also referred to as contig 22).

[0196] SEQ ID NO: 159 is the amino acid sequence encoded by SEQ ID NO: 158.

[0197] SEQ ID NO: 160 is the full-length cDNA sequence for L762P (also referred to as contig 17).

[0198] SEQ ID NO: 161 is the amino acid sequence encoded by SEQ ID NO: 160.

[0199] SEQ ID NO: 162 is the determined cDNA sequence for L515S.

[0200] SEQ ID NO: 163 is the full-length cDNA sequence of a first variant of L524S.

[0201] SEQ ID NO: 164 is the full-length cDNA sequence of a second variant of L524S.

[0202] SEQ ID NO: 165 is the amino acid sequence encoded by SEQ ID NO: 163.

[0203] SEQ ID NO: 166 is the amino acid sequence encoded by SEQ ID NO: 164.

[0204] SEQ ID NO: 167 is the full-length cDNA sequence of a first variant of L762P.

[0205] SEQ ID NO: 168 is the full-length cDNA sequence of a second variant of L762P.

[0206] SEQ ID NO: 169 is the amino acid sequence encoded by SEQ ID NO: 167.

[0207] SEQ ID NO: 170 is the amino acid sequence encoded by SEQ ID NO: 168.

[0208] SEQ ID NO: 171 is the full-length cDNA sequence for L773P (also referred to as contig 56).

[0209] SEQ ID NO: 172 is the amino acid sequence encoded by SEQ ID NO: 171.

[0210] SEQ ID NO: 173 is an extended cDNA sequence for L519S.

[0211] SEQ ID NO: 174 is the amino acid sequence encoded by SEQ ID NO: 174.

[0212] SEQ ID NO: 175 is the full-length cDNA sequence for L523S.

[0213] SEQ ID NO: 176 is the amino acid sequence encoded by SEQ ID NO: 175.

[0214] SEQ ID NO: 177 is the determined cDNA sequence for LST-sub5-7A.

[0215] SEQ ID NO: 178 is the determined cDNA sequence for LST-sub5-8G.

[0216] SEQ ID NO: 179 is the determined cDNA sequence for LST-sub5-8H.

[0217] SEQ ID NO: 180 is the determined cDNA sequence for LST-sub5-10B.

[0218] SEQ ID NO: 181 is the determined cDNA sequence for LST-sub5-10H.

[0219] SEQ ID NO: 182 is the determined cDNA sequence for LST-sub5-12B.

[0220] SEQ ID NO: 183 is the determined cDNA sequence for LST-sub5-11C.

[0221] SEQ ID NO: 184 is the determined cDNA sequence for LST-sub6-1c.

[0222] SEQ ID NO: 185 is the determined cDNA sequence for LST-sub6-2f.

[0223] SEQ ID NO: 186 is the determined cDNA sequence for LST-sub6-2G.

[0224] SEQ ID NO: 187 is the determined cDNA sequence for LST-sub6-4d.

[0225] SEQ ID NO: 188 is the determined cDNA sequence for LST-sub6-4e.

[0226] SEQ ID NO: 189 is the determined cDNA sequence for LST-sub6-4f.

[0227] SEQ ID NO: 190 is the determined cDNA sequence for LST-sub6-3h.

[0228] SEQ ID NO: 191 is the determined cDNA sequence for LST-sub6-5d.

[0229] SEQ ID NO: 192 is the determined cDNA sequence for LST-sub6-5h.

[0230] SEQ ID NO: 193 is the determined cDNA sequence for LST-sub6-6h.

[0231] SEQ ID NO: 194 is the determined cDNA sequence for LST-sub6-7a.

[0232] SEQ ID NO: 195 is the determined cDNA sequence for LST-sub6-8a.

[0233] SEQ ID NO: 196 is the determined cDNA sequence for LST-sub6-7d.

[0234] SEQ ID NO: 197 is the determined cDNA sequence for LST-sub6-7e.

[0235] SEQ ID NO: 198 is the determined cDNA sequence for LST-sub6-8e.

[0236] SEQ ID NO: 199 is the determined cDNA sequence for LST-sub6-7g.

[0237] SEQ ID NO: 200 is the determined cDNA sequence for LST-sub6-9f.

[0238] SEQ ID NO: 201 is the determined cDNA sequence for LST-sub6-9h.

[0239] SEQ ID NO: 202 is the determined cDNA sequence for LST-sub6-11b.

[0240] SEQ ID NO: 203 is the determined cDNA sequence for LST-sub6-11c.

[0241] SEQ ID NO: 204 is the determined cDNA sequence for LST-sub6-12c.

[0242] SEQ ID NO: 205 is the determined cDNA sequence for LST-sub6-12e.

[0243] SEQ ID NO: 206 is the determined cDNA sequence for LST-sub6-12f.

[0244] SEQ ID NO: 207 is the determined cDNA sequence for LST-sub6-11g.

[0245] SEQ ID NO: 208 is the determined cDNA sequence for LST-sub6-12g.

[0246] SEQ ID NO: 209 is the determined cDNA sequence for LST-sub6-12h.

[0247] SEQ ID NO: 210 is the determined cDNA sequence for LST-sub6-II-1a.

[0248] SEQ ID NO: 211 is the determined cDNA sequence for LST-sub6-II-2b.

[0249] SEQ ID NO: 212 is the determined cDNA sequence for LST-sub6-II-2g.

[0250] SEQ ID NO: 213 is the determined cDNA sequence for LST-sub6-II-1h.

[0251] SEQ ID NO: 214 is the determined cDNA sequence for LST-sub6-II-4a.

[0252] SEQ ID NO: 215 is the determined cDNA sequence for LST-sub6-II-4b.

[0253] SEQ ID NO: 216 is the determined cDNA sequence for LST-sub6-II-3e.

[0254] SEQ ID NO: 217 is the determined cDNA sequence for LST-sub6-II-4f.

[0255] SEQ ID NO: 218 is the determined cDNA sequence for LST-sub6-II-4g.

[0256] SEQ ID NO: 219 is the determined cDNA sequence for LST-sub6-II-4h.

[0257] SEQ ID NO: 220 is the determined cDNA sequence for LST-sub6-II-5c.

[0258] SEQ ID NO: 221 is the determined cDNA sequence for LST-sub6-II-5e.

[0259] SEQ ID NO: 222 is the determined cDNA sequence for LST-sub6-II-6f.

[0260] SEQ ID NO: 223 is the determined cDNA sequence for LST-sub6-II-5g.

[0261] SEQ ID NO: 224 is the determined cDNA sequence for LST-sub6-II-6g.

[0262] SEQ ID NO: 225 is the amino acid sequence for L528S.

[0263] SEQ ID NO: 226-251 are synthetic peptides derived from L762P.

[0264] SEQ ID NO: 252 is the expressed amino acid sequence of L514S.

[0265] SEQ ID NO: 253 is the DNA sequence corresponding to SEQ ID NO: 252.

[0266] SEQ ID NO: 254 is the DNA sequence of a L762P expression construct.

[0267] SEQ ID NO: 255 is the determined cDNA sequence for clone 23785.

[0268] SEQ ID NO: 256 is the determined cDNA sequence for clone 23786.

[0269] SEQ ID NO: 257 is the determined cDNA sequence for clone 23788.

[0270] SEQ ID NO: 258 is the determined cDNA sequence for clone 23790.

[0271] SEQ ID NO: 259 is the determined cDNA sequence for clone 23793.

[0272] SEQ ID NO: 260 is the determined cDNA sequence for clone 23794.

[0273] SEQ ID NO: 261 is the determined cDNA sequence for clone 23795.

[0274] SEQ ID NO: 262 is the determined cDNA sequence for clone 23796.

[0275] SEQ ID NO: 263 is the determined cDNA sequence for clone 23797.

[0276] SEQ ID NO: 264 is the determined cDNA sequence for clone 23798.

[0277] SEQ ID NO: 265 is the determined cDNA sequence for clone 23799.

[0278] SEQ ID NO: 266 is the determined cDNA sequence for clone 23800.

[0279] SEQ ID NO: 267 is the determined cDNA sequence for clone 23802.

[0280] SEQ ID NO: 268 is the determined cDNA sequence for clone 23803.

[0281] SEQ ID NO: 269 is the determined cDNA sequence for clone 23804.

[0282] SEQ ID NO: 270 is the determined cDNA sequence for clone 23805.

[0283] SEQ ID NO: 271 is the determined cDNA sequence for clone 23806.

[0284] SEQ ID NO: 272 is the determined cDNA sequence for clone 23807.

[0285] SEQ ID NO: 273 is the determined cDNA sequence for clone 23808.

[0286] SEQ ID NO: 274 is the determined cDNA sequence for clone 23809.

[0287] SEQ ID NO: 275 is the determined cDNA sequence for clone 23810.

[0288] SEQ ID NO: 276 is the determined cDNA sequence for clone 23811.

[0289] SEQ ID NO: 277 is the determined cDNA sequence for clone 23812.

[0290] SEQ ID NO: 278 is the determined cDNA sequence for clone 23813.

[0291] SEQ ID NO: 279 is the determined cDNA sequence for clone 23815.

[0292] SEQ ID NO: 280 is the determined cDNA sequence for clone 25298.

[0293] SEQ ID NO: 281 is the determined cDNA sequence for clone 25299.

[0294] SEQ ID NO: 282 is the determined cDNA sequence for clone 25300.

[0295] SEQ ID NO: 283 is the determined cDNA sequence for clone 25301

[0296] SEQ ID NO: 284 is the determined cDNA sequence for clone 25304

[0297] SEQ ID NO: 285 is the determined cDNA sequence for clone 25309.

[0298] SEQ ID NO: 286 is the determined cDNA sequence for clone 25312.

[0299] SEQ ID NO: 287 is the determined cDNA sequence for clone 25317.

[0300] SEQ ID NO: 288 is the determined cDNA sequence for clone 25321.

[0301] SEQ ID NO: 289 is the determined cDNA sequence for clone 25323.

[0302] SEQ ID NO: 290 is the determined cDNA sequence for clone 25327.

[0303] SEQ ID NO: 291 is the determined cDNA sequence for clone 25328.

[0304] SEQ ID NO: 292 is the determined cDNA sequence for clone 25332.

[0305] SEQ ID NO: 293 is the determined cDNA sequence for clone 25333.

[0306] SEQ ID NO: 294 is the determined cDNA sequence for clone 25336.

[0307] SEQ ID NO: 295 is the determined cDNA sequence for clone 25340.

[0308] SEQ ID NO: 296 is the determined cDNA sequence for clone 25342.

[0309] SEQ ID NO: 297 is the determined cDNA sequence for clone 25356.

[0310] SEQ ID NO: 298 is the determined cDNA sequence for clone 25357.

[0311] SEQ ID NO: 299 is the determined cDNA sequence for clone 25361.

[0312] SEQ ID NO: 300 is the determined cDNA sequence for clone 25363.

[0313] SEQ ID NO: 301 is the determined cDNA sequence for clone 25397.

[0314] SEQ ID NO: 302 is the determined cDNA sequence for clone 25402.

[0315] SEQ ID NO: 303 is the determined cDNA sequence for clone 25403.

[0316] SEQ ID NO: 304 is the determined cDNA sequence for clone 25405.

[0317] SEQ ID NO: 305 is the determined cDNA sequence for clone 25407.

[0318] SEQ ID NO: 306 is the determined cDNA sequence for clone 25409.

[0319] SEQ ID NO: 307 is the determined cDNA sequence for clone 25396.

[0320] SEQ ID NO: 308 is the determined cDNA sequence for clone 25414.

[0321] SEQ ID NO: 309 is the determined cDNA sequence for clone 25410.

[0322] SEQ ID NO: 310 is the determined cDNA sequence for clone 25406.

[0323] SEQ ID NO: 311 is the determined cDNA sequence for clone 25306.

[0324] SEQ ID NO: 312 is the determined cDNA sequence for clone 25362.

[0325] SEQ ID NO: 313 is the determined cDNA sequence for clone 25360.

[0326] SEQ ID NO: 314 is the determined cDNA sequence for clone 25398.

[0327] SEQ ID NO: 315 is the determined cDNA sequence for clone 25355.

[0328] SEQ ID NO: 316 is the determined cDNA sequence for clone 25351.

[0329] SEQ ID NO: 317 is the determined cDNA sequence for clone 25331.

[0330] SEQ ID NO: 318 is the determined cDNA sequence for clone 25338.

[0331] SEQ ID NO: 319 is the determined cDNA sequence for clone 25335.

[0332] SEQ ID NO: 320 is the determined cDNA sequence for clone 25329.

[0333] SEQ ID NO: 321 is the determined cDNA sequence for clone 25324.

[0334] SEQ ID NO: 322 is the determined cDNA sequence for clone 25322.

[0335] SEQ ID NO: 323 is the determined cDNA sequence for clone 25319.

[0336] SEQ ID NO: 324 is the determined cDNA sequence for clone 25316.

[0337] SEQ ID NO: 325 is the determined cDNA sequence for clone 25311.

[0338] SEQ ID NO: 326 is the determined cDNA sequence for clone 25310.

[0339] SEQ ID NO: 327 is the determined cDNA sequence for clone 25302.

[0340] SEQ ID NO: 328 is the determined cDNA sequence for clone 25315.

[0341] SEQ ID NO: 329 is the determined cDNA sequence for clone 25308.

[0342] SEQ ID NO: 330 is the determined cDNA sequence for clone 25303.

[0343] SEQ ID NO: 331-337 are the cDNA sequences of isoforms of the p53 tumor suppressor homologue, p63 (also referred to as L530S).

[0344] SEQ ID NO: 338-344 are the amino acid sequences encoded by SEQ ID NO: 331-337, respectively.

[0345] SEQ ID NO: 345 is a second cDNA sequence for the antigen L763P.

[0346] SEQ ID NO: 346 is the amino acid sequence encoded by the sequence of SEQ ID NO: 345.

[0347] SEQ ID NO: 347 is a determined full-length cDNA sequence for L523S.

[0348] SEQ ID NO: 348 is the amino acid sequence encoded by SEQ ID NO: 347.

[0349] SEQ ID NO: 349 is the cDNA sequence encoding the N-terminal portion of L773P.

[0350] SEQ ID NO: 350 is the amino acid sequence of the N-terminal portion of L773P.

[0351] SEQ ID NO: 351 is the DNA sequence for a fusion of Ra12 and the N-terminal portion of L763P

[0352] SEQ ID NO: 352 is the amino acid sequence of the fusion of Ra12 and the N-terminal portion of L763P

[0353] SEQ ID NO: 353 is the DNA sequence for a fusion of Ra12 and the C-terminal portion of L763P

[0354] SEQ ID NO: 354 is the amino acid sequence of the fusion of Ra12 and the C-terminal portion of L763P

[0355] SEQ ID NO: 355 is a primer.

[0356] SEQ ID NO: 356 is a primer.

[0357] SEQ ID NO: 357 is the protein sequence of expressed recombinant L762P.

[0358] SEQ ID NO: 358 is the DNA sequence of expressed recombinant L762P.

[0359] SEQ ID NO: 359 is a primer.

[0360] SEQ ID NO: 360 is a primer.

[0361] SEQ ID NO: 361 is the protein sequence of expressed recombinant L773P A.

[0362] SEQ ID NO: 362 is the DNA sequence of expressed recombinant L773P A.

[0363] SEQ ID NO: 363 is an epitope derived from clone L773P polypeptide.

[0364] SEQ ID NO: 364 is a polynucleotide encoding the polypeptide of SEQ ID NO: 363.

[0365] SEQ ID NO: 365 is an epitope derived from clone L773P polypeptide.

[0366] SEQ ID NO: 366 is a polynucleotide encoding the polypeptide of SEQ ID NO: 365.

[0367] SEQ ID NO: 367 is an epitope consisting of amino acids 571-590 of SEQ ID NO: 161, clone L762P.

[0368] SEQ ID NO: 368 is the full-length DNA sequence for contig 13 (SEQ ID NO: 125), also referred to as L761P.

[0369] SEQ ID NO: 369 is the protein sequence encoded by the DNA sequence of SEQ ID NO: 368.

[0370] SEQ ID NO: 370 is an L762P DNA sequence from nucleotides 2071-2130.

[0371] SEQ ID NO: 371 is an L762P DNA sequence from nucleotides 1441-1500.

[0372] SEQ ID NO: 372 is an L762P DNA sequence from nucleotides 1936-1955.

[0373] SEQ ID NO: 373 is an L762P DNA sequence from nucleotides 2620-2679.

[0374] SEQ ID NO: 374 is an L762P DNA sequence from nucleotides 1801-1860.

[0375] SEQ ID NO: 375 is an L762P DNA sequence from nucleotides 1531-1591.

[0376] SEQ ID NO: 376 is the amino acid sequence of the L762P peptide encoded by SEQ ID NO: 373.

[0377] SEQ ID NO: 377 is the amino acid sequence of the L762P peptide encoded by SEQ ID NO: 370.

[0378] SEQ ID NO: 378 is the amino acid sequence of the L762P peptide encoded by SEQ ID NO: 372.

[0379] SEQ ID NO: 379 is the amino acid sequence of the L762P peptide encoded by SEQ ID NO: 374.

[0380] SEQ ID NO: 380 is the amino acid sequence of the L762P peptide encoded by SEQ ID NO: 371.

[0381] SEQ ID NO: 381 is the amino acid sequence of the L762P peptide encoded by SEQ ID NO: 375.

[0382] SEQ ID NO: 382 is the amino acid sequence of an epitope of L762P.

[0383] SEQ ID NO: 383-386 are PCR primers.

[0384] SEQ ID NO: 387-395 are the amino acid sequences of L773P peptides.

[0385] SEQ ID NO: 396-419 are the amino acid sequences of L523S peptides.

[0386] SEQ ID NO: 420 is the determined cDNA sequence for clone #19014.

[0387] SEQ ID NO: 421 is the forward primer PDM-278 for the L514S-13160 coding region.

[0388] SEQ ID NO: 422 is the reverse primer PDM-278 for the L514S-13160 coding region.

[0389] SEQ ID NO: 423 is the amino acid sequence for the expressed recombinant L514S.

[0390] SEQ ID NO: 424 is the DNA coding sequence for the recombinant L514S.

[0391] SEQ ID NO: 425 is the forward primer PDM-414 for the L523S coding region.

[0392] SEQ ID NO: 426 is the reverse primer PDM-414 for the L523S coding region.

[0393] SEQ ID NO: 427 is the amino acid sequence for the expressed recombinant L523S.

[0394] SEQ ID NO: 428 is the DNA coding sequence for the recombinant L523S.

[0395] SEQ ID NO: 429 is the reverse primer PDM-279 for the L762PA coding region.

[0396] SEQ ID NO: 430 is the amino acid sequence for the expressed recombinant L762PA.

[0397] SEQ ID NO: 431 is the DNA coding sequence for the recombinant L762PA.

[0398] SEQ ID NO: 432 is the reverse primer PDM-300 for the L773P coding region.

[0399] SEQ ID NO: 433 is the amino acid sequence of the expressed recombinant L773P.

[0400] SEQ ID NO: 434 is the DNA coding sequence for the recombinant L773P.

[0401] SEQ ID NO: 435 is the forward primer for TCR Valpha8.

[0402] SEQ ID NO: 436 is the reverse primer for TCR Valpha8.

[0403] SEQ ID NO: 437 is the forward primer for TCR Vbeta8.

[0404] SEQ ID NO: 438 is the reverse primer for TCR Vbeta8.

[0405] SEQ ID NO: 439 is the TCR Valpha DNA sequence of the TCR clone specific for the lung antigen L762P.

[0406] SEQ ID NO: 440 is the TCR Vbeta DNA sequence of the TCR clone specific for the lung antigen L762P.

BRIEF DESCRIPTION OF THE FIGURES

[0407]FIG. 1 shows the sequences of eleven L773P peptides (SEQ ID NO: 363, 387, 388, 365 and 389-395, respectively).

[0408] FIGS. 2A-C show that three CD4+T cell lines (3C, 6G and 12B) recognized the appropriate L773P peptide as well as recombinant L773P and L773PA.

[0409] FIGS. 3A-D show that individual CD4+ T cell lines demonstrated cytokine release (IFN gamma) in response to the stimulating peptide but not the control peptide.

DETAILED DESCRIPTION OF THE INVENTION

[0410] The present invention is directed generally to compositions and their use in the therapy and diagnosis of cancer, particularly lung cancer. As described further below, illustrative compositions of the present invention include, but are not restricted to, polypeptides, particularly immunogenic polypeptides, polynucleotides encoding such polypeptides, antibodies and other binding agents, antigen presenting cells (APCs) and immune system cells (e.g., T cells).

[0411] The practice of the present invention will employ, unless indicated specifically to the contrary, conventional methods of virology, immunology, microbiology, molecular biology and recombinant DNA techniques within the skill of the art, many of which are described below for the purpose of illustration. Such techniques are explained fully in the literature. See, e.g., Sambrook, et al. Molecular Cloning: A Laboratory Manual (2nd Edition, 1989); Maniatis et al. Molecular Cloning: A Laboratory Manual (1982); DNA Cloning: A Practical Approach, vol. I & II (D. Glover, ed.); Oligonucleotide Synthesis (N. Gait, ed., 1984); Nucleic Acid Hybridization (B. Hames & S. Higgins, eds., 1985); Transcription and Translation (B. Hames & S. Higgins, eds., 1984); Animal Cell Culture (R. Freshney, ed., 1986); Perbal, A Practical Guide to Molecular Cloning (1984).

[0412] All publications, patents and patent applications cited herein, whether supra or infra, are hereby incorporated by reference in their entirety.

[0413] As used in this specification and the appended claims, the singular forms “a,” “an” and “the” include plural references unless the content clearly dictates otherwise.

[0414] Polypeptide Compositions

[0415] As used herein, the term “polypeptide” is used in its conventional meaning, i.e., as a sequence of amino acids. The polypeptides are not limited to a specific length of the product; thus, peptides, oligopeptides, and proteins are included within the definition of polypeptide, and such terms may be used interchangeably herein unless specifically indicated otherwise. This term also does not refer to or exclude post-expression modifications of the polypeptide, for example, glycosylations, acetylations, phosphorylations and the like, as well as other modifications known in the art, both naturally occurring and non-naturally occurring. A polypeptide may be an entire protein, or a subsequence thereof. Particular polypeptides of interest in the context of this invention are amino acid subsequences comprising epitopes, i.e., antigenic determinants substantially responsible for the immunogenic properties of a polypeptide and being capable of evoking an immune response.

[0416] Particularly illustrative polypeptides of the present invention comprise those encoded by a polynucleotide sequence set forth in any one of SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434, or a sequence that hybridizes under moderately stringent conditions, or, alternatively, under highly stringent conditions, to a polynucleotide sequence set forth in any one of SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434. Certain illustrative polypeptides of the invention comprise amino acid sequences as set forth in any one of SEQ ID NOs: 152, 155, 156, 165, 166, 169, 170, 172, 174, 176, 226-252, 338-344, 346, 350, 357, 361, 363, 365, 367, 369, 376-382, 387-419, 423, 427, 430 and 433.

[0417] The polypeptides of the present invention are sometimes herein referred to as lung tumor proteins or lung tumor polypeptides, as an indication that their identification has been based at least in part upon their increased levels of expression in lung tumor samples. Thus, a “lung tumor polypeptide” or “lung tumor protein,” refers generally to a polypeptide sequence of the present invention, or a polynucleotide sequence encoding such a polypeptide, that is expressed in a substantial proportion of lung tumor samples, for example preferably greater than about 20%, more preferably greater than about 30%, and most preferably greater than about 50% or more of lung tumor samples tested, at a level that is at least two fold, and preferably at least five fold, greater than the level of expression in normal tissues, as determined using a representative assay provided herein. A lung tumor polypeptide sequence of the invention, based upon its increased level of expression in tumor cells, has particular utility both as a diagnostic marker as well as a therapeutic target, as further described below.

[0418] In certain preferred embodiments, the polypeptides of the invention are immunogenic, i.e., they react detectably within an immunoassay (such as an ELISA or T-cell stimulation assay) with antisera and/or T-cells from a patient with lung cancer. Screening for immunogenic activity can be performed using techniques well known to the skilled artisan. For example, such screens can be performed using methods such as those described in Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988. In one illustrative example, a polypeptide may be immobilized on a solid support and contacted with patient sera to allow binding of antibodies within the sera to the immobilized polypeptide. Unbound sera may then be removed and bound antibodies detected using, for example, ¹²⁵I-labeled Protein A.

[0419] As would be recognized by the skilled artisan, immunogenic portions of the polypeptides disclosed herein are also encompassed by the present invention. An “immunogenic portion,” as used herein, is a fragment of an immunogenic polypeptide of the invention that itself is immunologically reactive (i.e., specifically binds) with the B-cells and/or T-cell surface antigen receptors that recognize the polypeptide. Immunogenic portions may generally be identified using well known techniques, such as those summarized in Paul, Fundamental Immunology, 3rd ed., 243-247 (Raven Press, 1993) and references cited therein. Such techniques include screening polypeptides for the ability to react with antigen-specific antibodies, antisera and/or T-cell lines or clones. As used herein, antisera and antibodies are “antigen-specific” if they specifically bind to an antigen (i.e., they react with the protein in an ELISA or other immunoassay, and do not react detectably with unrelated proteins). Such antisera and antibodies may be prepared as described herein, and using well-known techniques.

[0420] In one preferred embodiment, an immunogenic portion of a polypeptide of the present invention is a portion that reacts with antisera and/or T-cells at a level that is not substantially less than the reactivity of the full-length polypeptide (e.g., in an ELISA and/or T-cell reactivity assay). Preferably, the level of immunogenic activity of the immunogenic portion is at least about 50%, preferably at least about 70% and most preferably greater than about 90% of the immunogenicity for the full-length polypeptide. In some instances, preferred immunogenic portions will be identified that have a level of immunogenic activity greater than that of the corresponding full-length polypeptide, e.g., having greater than about 100% or 150% or more immunogenic activity.

[0421] In certain other embodiments, illustrative immunogenic portions may include peptides in which an N-terminal leader sequence and/or transmembrane domain have been deleted. Other illustrative immunogenic portions will contain a small N- and/or C-terminal deletion (e.g., 1-30 amino acids, preferably 5-15 amino acids), relative to the mature protein.

[0422] In another embodiment, a polypeptide composition of the invention may also comprise one or more polypeptides that are immunologically reactive with T cells and/or antibodies generated against a polypeptide of the invention, particularly a polypeptide having an amino acid sequence disclosed herein, or to an immunogenic fragment or variant thereof.

[0423] In another embodiment of the invention, polypeptides are provided that comprise one or more polypeptides that are capable of eliciting T cells and/or antibodies that are immunologically reactive with one or more polypeptides described herein, or one or more polypeptides encoded by contiguous nucleic acid sequences contained in the polynucleotide sequences disclosed herein, or immunogenic fragments or variants thereof, or to one or more nucleic acid sequences which hybridize to one or more of these sequences under conditions of moderate to high stringency.

[0424] The present invention, in another aspect, provides polypeptide fragments comprising at least about 5, 10, 15, 20, 25, 50, or 100 contiguous amino acids, or more, including all intermediate lengths, of a polypeptide compositions set forth herein, such as those set forth in SEQ ID NOs: 152, 155, 156, 165, 166, 169, 170, 172, 174, 176, 226-252, 338-344, 346, 350, 357, 361, 363, 365, 367, 369, 376-382 and 387-419, or those encoded by a polynucleotide sequence set forth in a sequence of SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434.

[0425] In another aspect, the present invention provides variants of the polypeptide compositions described herein. Polypeptide variants generally encompassed by the present invention will typically exhibit at least about 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% or more identity (determined as described below), along its length, to a polypeptide sequences set forth herein.

[0426] In one preferred embodiment, the polypeptide fragments and variants provide by the present invention are immunologically reactive with an antibody and/or T-cell that reacts with a full-length polypeptide specifically set for the herein.

[0427] In another preferred embodiment, the polypeptide fragments and variants provided by the present invention exhibit a level of immunogenic activity of at least about 50%, preferably at least about 70%, and most preferably at least about 90% or more of that exhibited by a full-length polypeptide sequence specifically set forth herein.

[0428] A polypeptide “variant,” as the term is used herein, is a polypeptide that typically differs from a polypeptide specifically disclosed herein in one or more substitutions, deletions, additions and/or insertions. Such variants may be naturally occurring or may be synthetically generated, for example, by modifying one or more of the above polypeptide sequences of the invention and evaluating their immunogenic activity as described herein and/or using any of a number of techniques well known in the art.

[0429] For example, certain illustrative variants of the polypeptides of the invention include those in which one or more portions, such as an N-terminal leader sequence or transmembrane domain, have been removed. Other illustrative variants include variants in which a small portion (e.g., 1-30 amino acids, preferably 5-15 amino acids) has been removed from the N- and/or C-terminal of the mature protein.

[0430] In many instances, a variant will contain conservative substitutions. A “conservative substitution” is one in which an amino acid is substituted for another amino acid that has similar properties, such that one skilled in the art of peptide chemistry would expect the secondary structure and hydropathic nature of the polypeptide to be substantially unchanged. As described above, modifications may be made in the structure of the polynucleotides and polypeptides of the present invention and still obtain a functional molecule that encodes a variant or derivative polypeptide with desirable characteristics, e.g., with immunogenic characteristics. When it is desired to alter the amino acid sequence of a polypeptide to create an equivalent, or even an improved, immunogenic variant or portion of a polypeptide of the invention, one skilled in the art will typically change one or more of the codons of the encoding DNA sequence according to Table 1.

[0431] For example, certain amino acids may be substituted for other amino acids in a protein structure without appreciable loss of interactive binding capacity with structures such as, for example, antigen-binding regions of antibodies or binding sites on substrate molecules. Since it is the interactive capacity and nature of a protein that defines that protein's biological functional activity, certain amino acid sequence substitutions can be made in a protein sequence, and, of course, its underlying DNA coding sequence, and nevertheless obtain a protein with like properties. It is thus contemplated that various changes may be made in the peptide sequences of the disclosed compositions, or corresponding DNA sequences which encode said peptides without appreciable loss of their biological utility or activity. TABLE 1 Amino Acids Codons Alanine Ala A GCA GCC GCG GCU Cysteine Cys C UGC UGU Aspartic acid Asp D GAC GAU Glutamic acid Glu E GAA GAG Phenylalanine Phe F UUC UUU Glycine Gly G GGA GGC GGG GGU Histidine His H CAC CAU Isoleucine Ile I AUA AUC AUU Lysine Lys K AAA AAG Leucine Leu L UUA UUG CUA CUC CUG CUU Methionine Met M AUG Asparagine Asn N AAC AAU Proline Pro P CCA CCC CCG CCU Glutamine Gln Q CAA CAG Arginine Arg R AGA AGG CGA CGC CGG CGU Serine Ser S AGC AGU UCA UCC UCG UCU Threonine Thr T ACA ACC ACG ACU Valine Val V GUA GUC GUG GUU Tryptophan Trp W UGG Tyrosine Tyr Y UAC UAU

[0432] In making such changes, the hydropathic index of amino acids may be considered. The importance of the hydropathic amino acid index in conferring interactive biologic function on a protein is generally understood in the art (Kyte and Doolittle, 1982, incorporated herein by reference). It is accepted that the relative hydropathic character of the amino acid contributes to the secondary structure of the resultant protein, which in turn defines the interaction of the protein with other molecules, for example, enzymes, substrates, receptors, DNA, antibodies, antigens, and the like. Each amino acid has been assigned a hydropathic index on the basis of its hydrophobicity and charge characteristics (Kyte and Doolittle, 1982). These values are: isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8); cysteine/cystine (+2.5); methionine (+1.9); alanine (+1.8); glycine (−0.4); threonine (−0.7); serine (−0.8); tryptophan (−0.9); tyrosine (−1.3); proline (−1.6); histidine (−3.2); glutamate (−3.5); glutamine (−3.5); aspartate (−3.5); asparagine (−3.5); lysine (−3.9); and arginine (−4.5).

[0433] It is known in the art that certain amino acids may be substituted by other amino acids having a similar hydropathic index or score and still result in a protein with similar biological activity, i.e., still obtain a biological functionally equivalent protein. In making such changes, the substitution of amino acids whose hydropathic indices are within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred. It is also understood in the art that the substitution of like amino acids can be made effectively on the basis of hydrophilicity. U.S. Pat. No. 4,554,101 (specifically incorporated herein by reference in its entirety), states that the greatest local average hydrophilicity of a protein, as governed by the hydrophilicity of its adjacent amino acids, correlates with a biological property of the protein.

[0434] As detailed in U.S. Pat. No. 4,554,101, the following hydrophilicity values have been assigned to amino acid residues: arginine (+3.0); lysine (+3.0); aspartate (+3.0±1); glutamate (+3.0±1); serine (+0.3); asparagine (+0.2); glutamine (+0.2); glycine (0); threonine (−0.4); proline (−0.5±1); alanine (−0.5); histidine (−0.5); cysteine (−1.0); methionine (−1.3); valine (−1.5); leucine (−1.8); isoleucine (−1.8); tyrosine (−2.3); phenylalanine (−2.5); tryptophan (−3.4). It is understood that an amino acid can be substituted for another having a similar hydrophilicity value and still obtain a biologically equivalent, and in particular, an immunologically equivalent protein. In such changes, the substitution of amino acids whose hydrophilicity values are within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred.

[0435] As outlined above, amino acid substitutions are generally therefore based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions that take various of the foregoing characteristics into consideration are well known to those of skill in the art and include: arginine and lysine; glutamate and aspartate; serine and threonine; glutamine and asparagine; and valine, leucine and isoleucine.

[0436] In addition, any polynucleotide may be further modified to increase stability in vivo. Possible modifications include, but are not limited to, the addition of flanking sequences at the 5′ and/or 3′ ends; the use of phosphorothioate or 2′ O-methyl rather than phosphodiesterase linkages in the backbone; and/or the inclusion of nontraditional bases such as inosine, queosine and wybutosine, as well as acetyl- methyl-, thio- and other modified forms of adenine, cytidine, guanine, thymine and uridine.

[0437] Amino acid substitutions may further be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity and/or the amphipathic nature of the residues. For example, negatively charged amino acids include aspartic acid and glutamic acid; positively charged amino acids include lysine and arginine; and amino acids with uncharged polar head groups having similar hydrophilicity values include leucine, isoleucine and valine; glycine and alanine; asparagine and glutamine; and serine, threonine, phenylalanine and tyrosine. Other groups of amino acids that may represent conservative changes include: (1) ala, pro, gly, glu, asp, gln, asn, ser, thr; (2) cys, ser, tyr, thr; (3) val, ile, leu, met, ala, phe; (4) lys, arg, his; and (5) phe, tyr, trp, his. A variant may also, or alternatively, contain nonconservative changes. In a preferred embodiment, variant polypeptides differ from a native sequence by substitution, deletion or addition of five amino acids or fewer. Variants may also (or alternatively) be modified by, for example, the deletion or addition of amino acids that have minimal influence on the immunogenicity, secondary structure and hydropathic nature of the polypeptide.

[0438] As noted above, polypeptides may comprise a signal (or leader) sequence at the N-terminal end of the protein, which co-translationally or post-translationally directs transfer of the protein. The polypeptide may also be conjugated to a linker or other sequence for ease of synthesis, purification or identification of the polypeptide (e.g., poly-His), or to enhance binding of the polypeptide to a solid support. For example, a polypeptide may be conjugated to an immunoglobulin Fc region.

[0439] When comparing polypeptide sequences, two sequences are said to be “identical” if the sequence of amino acids in the two sequences is the same when aligned for maximum correspondence, as described below. Comparisons between two sequences are typically performed by comparing the sequences over a comparison window to identify and compare local regions of sequence similarity. A “comparison window” as used herein, refers to a segment of at least about 20 contiguous positions, usually 30 to about 75, 40 to about 50, in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned.

[0440] Optimal alignment of sequences for comparison may be conducted using the Megalign program in the Lasergene suite of bioinformatics software (DNASTAR, Inc., Madison, Wis.), using default parameters. This program embodies several alignment schemes described in the following references: Dayhoff, M. O. (1978) A model of evolutionary change in proteins - Matrices for detecting distant relationships. In Dayhoff, M. O. (ed.) Atlas of Protein Sequence and Structure, National Biomedical Research Foundation, Washington D.C. Vol. 5, Suppl. 3, pp. 345-358; Hein J. (1990) Unified Approach to Alignment and Phylogenes pp. 626-645 Methods in Enzymology vol. 183, Academic Press, Inc., San Diego, Calif.; Higgins, D. G. and Sharp, P. M. (1989) CABIOS 5:151-153; Myers, E. W. and Muller W. (1988) CABIOS 4:11-17; Robinson, E. D. (1971) Comb. Theor 11:105; Santou, N. Nes, M. (1987) Mol. Biol. Evol. 4:406-425; Sneath, P. H. A. and Sokal, R. R. (1973) Numerical Taxonomy—the Principles and Practice of Numerical Taxonomy, Freeman Press, San Francisco, Calif.; Wilbur, W. J. and Lipman, D. J. (1983) Proc. Natl. Acad., Sci. USA 80:726-730.

[0441] Alternatively, optimal alignment of sequences for comparison may be conducted by the local identity algorithm of Smith and Waterman (1981) Add. APL. Math 2:482, by the identity alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity methods of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85: 2444, by computerized implementations of these algorithms (GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.), or by inspection.

[0442] One preferred example of algorithms that are suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al. (1977) Nucl. Acids Res. 25:3389-3402 and Altschul et al. (1990) J. Mol. Biol. 215:403-410, respectively. BLAST and BLAST 2.0 can be used, for example with the parameters described herein, to determine percent sequence identity for the polynucleotides and polypeptides of the invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information. For amino acid sequences, a scoring matrix can be used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T and X determine the sensitivity and speed of the alignment.

[0443] In one preferred approach, the “percentage of sequence identity” is determined by comparing two optimally aligned sequences over a window of comparison of at least 20 positions, wherein the portion of the polypeptide sequence in the comparison window may comprise additions or deletions (i.e., gaps) of 20 percent or less, usually 5 to 15 percent, or 10 to 12 percent, as compared to the reference sequences (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the reference sequence (i.e., the window size) and multiplying the results by 100 to yield the percentage of sequence identity.

[0444] Within other illustrative embodiments, a polypeptide may be a fusion polypeptide that comprises multiple polypeptides as described herein, or that comprises at least one polypeptide as described herein and an unrelated sequence, such as a known tumor protein. A fusion partner may, for example, assist in providing T helper epitopes (an immunological fusion partner), preferably T helper epitopes recognized by humans, or may assist in expressing the protein (an expression enhancer) at higher yields than the native recombinant protein. Certain preferred fusion partners are both immunological and expression enhancing fusion partners. Other fusion partners may be selected so as to increase the solubility of the polypeptide or to enable the polypeptide to be targeted to desired intracellular compartments. Still further fusion partners include affinity tags, which facilitate purification of the polypeptide.

[0445] Fusion polypeptides may generally be prepared using standard techniques, including chemical conjugation. Preferably, a fusion polypeptide is expressed as a recombinant polypeptide, allowing the production of increased levels, relative to a non-fused polypeptide, in an expression system. Briefly, DNA sequences encoding the polypeptide components may be assembled separately, and ligated into an appropriate expression vector. The 3′ end of the DNA sequence encoding one polypeptide component is ligated, with or without a peptide linker, to the 5′ end of a DNA sequence encoding the second polypeptide component so that the reading frames of the sequences are in phase. This permits translation into a single fusion polypeptide that retains the biological activity of both component polypeptides.

[0446] A peptide linker sequence may be employed to separate the first and second polypeptide components by a distance sufficient to ensure that each polypeptide folds into its secondary and tertiary structures. Such a peptide linker sequence is incorporated into the fusion polypeptide using standard techniques well known in the art. Suitable peptide linker sequences may be chosen based on the following factors: (1) their ability to adopt a flexible extended conformation; (2) their inability to adopt a secondary structure that could interact with functional epitopes on the first and second polypeptides; and (3) the lack of hydrophobic or charged residues that might react with the polypeptide functional epitopes. Preferred peptide linker sequences contain Gly, Asn and Ser residues. Other near neutral amino acids, such as Thr and Ala may also be used in the linker sequence. Amino acid sequences which may be usefully employed as linkers include those disclosed in Maratea et al., Gene 40:39-46, 1985; Murphy et al., Proc. Natl. Acad. Sci. USA 83:8258-8262, 1986; U.S. Pat. No. 4,935,233 and U.S. Pat. No. 4,751,180. The linker sequence may generally be from 1 to about 50 amino acids in length. Linker sequences are not required when the first and second polypeptides have non-essential N-terminal amino acid regions that can be used to separate the functional domains and prevent steric interference.

[0447] The ligated DNA sequences are operably linked to suitable transcriptional or translational regulatory elements. The regulatory elements responsible for expression of DNA are located only 5′ to the DNA sequence encoding the first polypeptides. Similarly, stop codons required to end translation and transcription termination signals are only present 3′ to the DNA sequence encoding the second polypeptide.

[0448] The fusion polypeptide can comprise a polypeptide as described herein together with an unrelated immunogenic protein, such as an immunogenic protein capable of eliciting a recall response. Examples of such proteins include tetanus, tuberculosis and hepatitis proteins (see, for example, Stoute et al. New Engl. J Med., 336:86-91, 1997).

[0449] In one preferred embodiment, the immunological fusion partner is derived from a Mycobacterium sp., such as a Mycobacterium tuberculosis-derived Ra12 fragment. Ra12 compositions and methods for their use in enhancing the expression and/or immunogenicity of heterologous polynucleotide/polypeptide sequences is described in U.S. patent application Ser. No. 60/158,585, the disclosure of which is incorporated herein by reference in its entirety. Briefly, Ra12 refers to a polynucleotide region that is a subsequence of a Mycobacterium tuberculosis MTB32A nucleic acid. MTB32A is a serine protease of 32 KD molecular weight encoded by a gene in virulent and avirulent strains of M. tuberculosis. The nucleotide sequence and amino acid sequence of MTB32A have been described (for example, U.S. patent application Ser. No. 60/158,585; see also, Skeiky et al., Infection and Immun. (1999) 67:3998-4007, incorporated herein by reference). C-terminal fragments of the MTB32A coding sequence express at high levels and remain as a soluble polypeptides throughout the purification process. Moreover, Ra12 may enhance the immunogenicity of heterologous immunogenic polypeptides with which it is fused. One preferred Ra12 fusion polypeptide comprises a 14 KD C-terminal fragment corresponding to amino acid residues 192 to 323 of MTB32A. Other preferred Ra12 polynucleotides generally comprise at least about 15 consecutive nucleotides, at least about 30 nucleotides, at least about 60 nucleotides, at least about 100 nucleotides, at least about 200 nucleotides, or at least about 300 nucleotides that encode a portion of a Ra12 polypeptide. Ra12 polynucleotides may comprise a native sequence (i.e., an endogenous sequence that encodes a Ra12 polypeptide or a portion thereof) or may comprise a variant of such a sequence. Ra12 polynucleotide variants may contain one or more substitutions, additions, deletions and/or insertions such that the biological activity of the encoded fusion polypeptide is not substantially diminished, relative to a fusion polypeptide comprising a native Ra12 polypeptide. Variants preferably exhibit at least about 70% identity, more preferably at least about 80% identity and most preferably at least about 90% identity to a polynucleotide sequence that encodes a native Ra12 polypeptide or a portion thereof.

[0450] Within other preferred embodiments, an immunological fusion partner is derived from protein D, a surface protein of the gram-negative bacterium Haemophilus influenza B (WO 91/18926). Preferably, a protein D derivative comprises approximately the first third of the protein (e.g., the first N-terminal 100-110 amino acids), and a protein D derivative may be lipidated. Within certain preferred embodiments, the first 109 residues of a Lipoprotein D fusion partner is included on the N-terminus to provide the polypeptide with additional exogenous T-cell epitopes and to increase the expression level in E. coli (thus functioning as an expression enhancer). The lipid tail ensures optimal presentation of the antigen to antigen presenting cells. Other fusion partners include the non-structural protein from influenzae virus, NS1 (hemaglutinin). Typically, the N-terminal 81 amino acids are used, although different fragments that include T-helper epitopes may be used.

[0451] In another embodiment, the immunological fusion partner is the protein known as LYTA, or a portion thereof (preferably a C-terminal portion). LYTA is derived from Streptococcus pneumoniae, which synthesizes an N-acetyl-L-alanine amidase known as amidase LYTA (encoded by the LytA gene; Gene 43:265-292, 1986). LYTA is an autolysin that specifically degrades certain bonds in the peptidoglycan backbone. The C-terminal domain of the LYTA protein is responsible for the affinity to the choline or to some choline analogues such as DEAE. This property has been exploited for the development of E. coli C-LYTA expressing plasmids useful for expression of fusion proteins. Purification of hybrid proteins containing the C-LYTA fragment at the amino terminus has been described (see Biotechnology 10:795-798, 1992). Within a preferred embodiment, a repeat portion of LYTA may be incorporated into a fusion polypeptide. A repeat portion is found in the C-terminal region starting at residue 178. A particularly preferred repeat portion incorporates residues 188-305.

[0452] Yet another illustrative embodiment involves fusion polypeptides, and the polynucleotides encoding them, wherein the fusion partner comprises a targeting signal capable of directing a polypeptide to the endosomal/lysosomal compartment, as described in U.S. Pat. No. 5,633,234. An immunogenic polypeptide of the invention, when fused with this targeting signal, will associate more efficiently with MHC class II molecules and thereby provide enhanced in vivo stimulation of CD4⁺ T-cells specific for the polypeptide.

[0453] Polypeptides of the invention are prepared using any of a variety of well known synthetic and/or recombinant techniques, the latter of which are further described below. Polypeptides, portions and other variants generally less than about 150 amino acids can be generated by synthetic means, using techniques well known to those of ordinary skill in the art. In one illustrative example, such polypeptides are synthesized using any of the commercially available solid-phase techniques, such as the Merrifield solid-phase synthesis method, where amino acids are sequentially added to a growing amino acid chain. See Merrifield, J. Am. Chem. Soc. 85:2149-2146, 1963. Equipment for automated synthesis of polypeptides is commercially available from suppliers such as Perkin Elmer/Applied BioSystems Division (Foster City, Calif.), and may be operated according to the manufacturer's instructions.

[0454] In general, polypeptide compositions (including fusion polypeptides) of the invention are isolated. An “isolated” polypeptide is one that is removed from its original environment. For example, a naturally-occurring protein or polypeptide is isolated if it is separated from some or all of the coexisting materials in the natural system. Preferably, such polypeptides are also purified, e.g., are at least about 90% pure, more preferably at least about 95% pure and most preferably at least about 99% pure.

[0455] Polynucleotide Compositions

[0456] The present invention, in other aspects, provides polynucleotide compositions. The terms “DNA” and “polynucleotide” are used essentially interchangeably herein to refer to a DNA molecule that has been isolated free of total genomic DNA of a particular species. “Isolated,” as used herein, means that a polynucleotide is substantially away from other coding sequences, and that the DNA molecule does not contain large portions of unrelated coding DNA, such as large chromosomal fragments or other functional genes or polypeptide coding regions. Of course, this refers to the DNA molecule as originally isolated, and does not exclude genes or coding regions later added to the segment by the hand of man.

[0457] As will be understood by those skilled in the art, the polynucleotide compositions of this invention can include genomic sequences, extra-genomic and plasmid-encoded sequences and smaller engineered gene segments that express, or may be adapted to express, proteins, polypeptides, peptides and the like. Such segments may be naturally isolated, or modified synthetically by the hand of man.

[0458] As will be also recognized by the skilled artisan, polynucleotides of the invention may be single-stranded (coding or antisense) or double-stranded, and may be DNA (genomic, cDNA or synthetic) or RNA molecules. RNA molecules may include HnRNA molecules, which contain introns and correspond to a DNA molecule in a one-to-one manner, and mRNA molecules, which do not contain introns. Additional coding or non-coding sequences may, but need not, be present within a polynucleotide of the present invention, and a polynucleotide may, but need not, be linked to other molecules and/or support materials.

[0459] Polynucleotides may comprise a native sequence (i.e., an endogenous sequence that encodes a polypeptide/protein of the invention or a portion thereof) or may comprise a sequence that encodes a variant or derivative, preferably and immunogenic variant or derivative, of such a sequence.

[0460] Therefore, according to another aspect of the present invention, polynucleotide compositions are provided that comprise some or all of a polynucleotide sequence set forth in any one of SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434, complements of a polynucleotide sequence set forth in any one of SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434, and degenerate variants of a polynucleotide sequence set forth in any one of SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434. In certain preferred embodiments, the polynucleotide sequences set forth herein encode immunogenic polypeptides, as described above.

[0461] In other related embodiments, the present invention provides polynucleotide variants having substantial identity to the sequences disclosed herein in SEQ ID NOs: 1-3, 6-8, 10-13, 15-27, 29, 30, 32, 34-49, 51, 52, 54, 55, 57-59, 61-69, 71, 73, 74, 77, 78, 80-82, 84, 86-96, 107-109, 111, 113, 125, 127, 128, 129, 131-133, 142, 144, 148-151, 153, 154, 157, 158, 160, 167, 168, 171, 179, 182, 184-186, 188-191, 193, 194, 198-207, 209, 210, 213, 214, 217, 220-224, 253-337, 345, 347, 349, 358, 362, 364, 365, 368, 370-375, 420, 424, 428, 431 and 434, for example those comprising at least 70% sequence identity, preferably at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% or higher, sequence identity compared to a polynucleotide sequence of this invention using the methods described herein, (e.g., BLAST analysis using standard parameters, as described below). One skilled in this art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by two nucleotide sequences by taking into account codon degeneracy, amino acid similarity, reading frame positioning and the like.

[0462] Typically, polynucleotide variants will contain one or more substitutions, additions, deletions and/or insertions, preferably such that the immunogenicity of the polypeptide encoded by the variant polynucleotide is not substantially diminished relative to a polypeptide encoded by a polynucleotide sequence specifically set forth herein). The term “variants” should also be understood to encompasses homologous genes of xenogenic origin.

[0463] In additional embodiments, the present invention provides polynucleotide fragments comprising various lengths of contiguous stretches of sequence identical to or complementary to one or more of the sequences disclosed herein. For example, polynucleotides are provided by this invention that comprise at least about 10, 15, 20, 30, 40, 50, 75, 100, 150, 200, 300, 400, 500 or 1000 or more contiguous nucleotides of one or more of the sequences disclosed herein as well as all intermediate lengths there between. It will be readily understood that “intermediate lengths”, in this context, means any length between the quoted values, such as 16, 17, 18, 19, etc.; 21, 22, 23, etc.; 30, 31, 32, etc.; 50, 51, 52, 53, etc.; 100, 101, 102, 103, etc.; 150, 151, 152, 153, etc.; including all integers through 200-500; 500-1,000, and the like.

[0464] In another embodiment of the invention, polynucleotide compositions are provided that are capable of hybridizing under moderate to high stringency conditions to a polynucleotide sequence provided herein, or a fragment thereof, or a complementary sequence thereof. Hybridization techniques are well known in the art of molecular biology. For purposes of illustration, suitable moderately stringent conditions for testing the hybridization of a polynucleotide of this invention with other polynucleotides include prewashing in a solution of 5×SSC, 0.5% SDS, 1.0 mM EDTA (pH 8.0); hybridizing at 50° C.-60° C., 5×SSC, overnight; followed by washing twice at 65° C. for 20 minutes with each of 2×, 0.5× and 0.2×SSC containing 0.1% SDS. One skilled in the art will understand that the stringency of hybridization can be readily manipulated, such as by altering the salt content of the hybridization solution and/or the temperature at which the hybridization is performed. For example, in another embodiment, suitable highly stringent hybridization conditions include those described above, with the exception that the temperature of hybridization is increased, e.g., to 60-65° C. or 65-70° C.

[0465] In certain preferred embodiments, the polynucleotides described above, e.g., polynucleotide variants, fragments and hybridizing sequences, encode polypeptides that are immunologically cross-reactive with a polypeptide sequence specifically set forth herein. In other preferred embodiments, such polynucleotides encode polypeptides that have a level of immunogenic activity of at least about 50%, preferably at least about 70%, and more preferably at least about 90% of that for a polypeptide sequence specifically set forth herein.

[0466] The polynucleotides of the present invention, or fragments thereof, regardless of the length of the coding sequence itself, may be combined with other DNA sequences, such as promoters, polyadenylation signals, additional restriction enzyme sites, multiple cloning sites, other coding segments, and the like, such that their overall length may vary considerably. It is therefore contemplated that a nucleic acid fragment of almost any length may be employed, with the total length preferably being limited by the ease of preparation and use in the intended recombinant DNA protocol. For example, illustrative polynucleotide segments with total lengths of about 10,000, about 5000, about 3000, about 2,000, about 1,000, about 500, about 200, about 100, about 50 base pairs in length, and the like, (including all intermediate lengths) are contemplated to be useful in many implementations of this invention.

[0467] When comparing polynucleotide sequences, two sequences are said to be “identical” if the sequence of nucleotides in the two sequences is the same when aligned for maximum correspondence, as described below. Comparisons between two sequences are typically performed by comparing the sequences over a comparison window to identify and compare local regions of sequence similarity. A “comparison window” as used herein, refers to a segment of at least about 20 contiguous positions, usually 30 to about 75, 40 to about 50, in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned.

[0468] Optimal alignment of sequences for comparison may be conducted using the Megalign program in the Lasergene suite of bioinformatics software (DNASTAR, Inc., Madison, Wis.), using default parameters. This program embodies several alignment schemes described in the following references: Dayhoff, M. O. (1978) A model of evolutionary change in proteins—Matrices for detecting distant relationships. In Dayhoff, M. O. (ed.) Atlas of Protein Sequence and Structure, National Biomedical Research Foundation, Washington D.C. Vol. 5, Suppl. 3, pp. 345-358; Hein J. (1990) Unified Approach to Alignment and Phylogenes pp. 626-645 Methods in Enzymology vol. 183, Academic Press, Inc., San Diego, Calif.; Higgins, D. G. and Sharp, P. M. (1989) CABIOS 5:151-153; Myers, E. W. and Muller W. (1988) CABIOS 4:11-17; Robinson, E. D. (1971) Comb. Theor 11:105; Santou, N. Nes, M. (1987) Mol. Biol. Evol. 4:406-425; Sneath, P. H. A. and Sokal, R. R. (1973) Numerical Taxonomy—the Principles and Practice of Numerical Taxonomy, Freeman Press, San Francisco, Calif.; Wilbur, W. J. and Lipman, D. J. (1983) Proc. Natl. Acad., Sci. USA 80:726-730.

[0469] Alternatively, optimal alignment of sequences for comparison may be conducted by the local identity algorithm of Smith and Waterman (1981) Add. APL. Math 2:482, by the identity alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity methods of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85: 2444, by computerized implementations of these algorithms (GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.), or by inspection.

[0470] One preferred example of algorithms that are suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al. (1977) Nucl. Acids Res. 25:3389-3402 and Altschul et al. (1990) J. Mol. Biol. 215:403-410, respectively. BLAST and BLAST 2.0 can be used, for example with the parameters described herein, to determine percent sequence identity for the polynucleotides of the invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information. In one illustrative example, cumulative scores can be calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always >0) and N (penalty score for mismatching residues; always <0). Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, and expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff and Henikoff (1989) Proc. Natl. Acad. Sci. USA 89:10915) alignments, (B) of 50, expectation (E) of 10, M=5, N=−4 and a comparison of both strands.

[0471] Preferably, the “percentage of sequence identity” is determined by comparing two optimally aligned sequences over a window of comparison of at least 20 positions, wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) of 20 percent or less, usually 5 to 15 percent, or 10 to 12 percent, as compared to the reference sequences (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid bases occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the reference sequence (i.e., the window size) and multiplying the results by 100 to yield the percentage of sequence identity.

[0472] It will be appreciated by those of ordinary skill in the art that, as a result of the degeneracy of the genetic code, there are many nucleotide sequences that encode a polypeptide as described herein. Some of these polynucleotides bear minimal homology to the nucleotide sequence of any native gene. Nonetheless, polynucleotides that vary due to differences in codon usage are specifically contemplated by the present invention. Further, alleles of the genes comprising the polynucleotide sequences provided herein are within the scope of the present invention. Alleles are endogenous genes that are altered as a result of one or more mutations, such as deletions, additions and/or substitutions of nucleotides. The resulting mRNA and protein may, but need not, have an altered structure or function. Alleles may be identified using standard techniques (such as hybridization, amplification and/or database sequence comparison).

[0473] Therefore, in another embodiment of the invention, a mutagenesis approach, such as site-specific mutagenesis, is employed for the preparation of immunogenic variants and/or derivatives of the polypeptides described herein. By this approach, specific modifications in a polypeptide sequence can be made through mutagenesis of the underlying polynucleotides that encode them. These techniques provides a straightforward approach to prepare and test sequence variants, for example, incorporating one or more of the foregoing considerations, by introducing one or more nucleotide sequence changes into the polynucleotide.

[0474] Site-specific mutagenesis allows the production of mutants through the use of specific oligonucleotide sequences which encode the DNA sequence of the desired mutation, as well as a sufficient number of adjacent nucleotides, to provide a primer sequence of sufficient size and sequence complexity to form a stable duplex on both sides of the deletion junction being traversed. Mutations may be employed in a selected polynucleotide sequence to improve, alter, decrease, modify, or otherwise change the properties of the polynucleotide itself, and/or alter the properties, activity, composition, stability, or primary sequence of the encoded polypeptide.

[0475] In certain embodiments of the present invention, the inventors contemplate the mutagenesis of the disclosed polynucleotide sequences to alter one or more properties of the encoded polypeptide, such as the immunogenicity of a polypeptide vaccine. The techniques of site-specific mutagenesis are well-known in the art, and are widely used to create variants of both polypeptides and polynucleotides. For example, site-specific mutagenesis is often used to alter a specific portion of a DNA molecule. In such embodiments, a primer comprising typically about 14 to about 25 nucleotides or so in length is employed, with about 5 to about 10 residues on both sides of the junction of the sequence being altered.

[0476] As will be appreciated by those of skill in the art, site-specific mutagenesis techniques have often employed a phage vector that exists in both a single stranded and double stranded form. Typical vectors useful in site-directed mutagenesis include vectors such as the M13 phage. These phage are readily commercially-available and their use is generally well-known to those skilled in the art. Double-stranded plasmids are also routinely employed in site directed mutagenesis that eliminates the step of transferring the gene of interest from a plasmid to a phage.

[0477] In general, site-directed mutagenesis in accordance herewith is performed by first obtaining a single-stranded vector or melting apart of two strands of a double-stranded vector that includes within its sequence a DNA sequence that encodes the desired peptide. An oligonucleotide primer bearing the desired mutated sequence is prepared, generally synthetically. This primer is then annealed with the single-stranded vector, and subjected to DNA polymerizing enzymes such as E. coli polymerase I Klenow fragment, in order to complete the synthesis of the mutation-bearing strand. Thus, a heteroduplex is formed wherein one strand encodes the original non-mutated sequence and the second strand bears the desired mutation. This heteroduplex vector is then used to transform appropriate cells, such as E. coli cells, and clones are selected which include recombinant vectors bearing the mutated sequence arrangement.

[0478] The preparation of sequence variants of the selected peptide-encoding DNA segments using site-directed mutagenesis provides a means of producing potentially useful species and is not meant to be limiting as there are other ways in which sequence variants of peptides and the DNA sequences encoding them may be obtained. For example, recombinant vectors encoding the desired peptide sequence may be treated with mutagenic agents, such as hydroxylamine, to obtain sequence variants. Specific details regarding these methods and protocols are found in the teachings of Maloy et al., 1994; Segal, 1976; Prokop and Bajpai, 1991; Kuby, 1994; and Maniatis et al., 1982, each incorporated herein by reference, for that purpose.

[0479] As used herein, the term “oligonucleotide directed mutagenesis procedure” refers to template-dependent processes and vector-mediated propagation which result in an increase in the concentration of a specific nucleic acid molecule relative to its initial concentration, or in an increase in the concentration of a detectable signal, such as amplification. As used herein, the term “oligonucleotide directed mutagenesis procedure” is intended to refer to a process that involves the template-dependent extension of a primer molecule. The term template dependent process refers to nucleic acid synthesis of an RNA or a DNA molecule wherein the sequence of the newly synthesized strand of nucleic acid is dictated by the well-known rules of complementary base pairing (see, for example, Watson, 1987). Typically, vector mediated methodologies involve the introduction of the nucleic acid fragment into a DNA or RNA vector, the clonal amplification of the vector, and the recovery of the amplified nucleic acid fragment. Examples of such methodologies are provided by U.S. Pat. No. 4,237,224, specifically incorporated herein by reference in its entirety.

[0480] In another approach for the production of polypeptide variants of the present invention, recursive sequence recombination, as described in U.S. Pat. No. 5,837,458, may be employed. In this approach, iterative cycles of recombination and screening or selection are performed to “evolve” individual polynucleotide variants of the invention having, for example, enhanced immunogenic activity.

[0481] In other embodiments of the present invention, the polynucleotide sequences provided herein can be advantageously used as probes or primers for nucleic acid hybridization. As such, it is contemplated that nucleic acid segments that comprise a sequence region of at least about 15 nucleotide long contiguous sequence that has the same sequence as, or is complementary to, a 15 nucleotide long contiguous sequence disclosed herein will find particular utility. Longer contiguous identical or complementary sequences, e.g., those of about 20, 30, 40, 50, 100, 200, 500, 1000 (including all intermediate lengths) and even up to full length sequences will also be of use in certain embodiments.

[0482] The ability of such nucleic acid probes to specifically hybridize to a sequence of interest will enable them to be of use in detecting the presence of complementary sequences in a given sample. However, other uses are also envisioned, such as the use of the sequence information for the preparation of mutant species primers, or primers for use in preparing other genetic constructions.

[0483] Polynucleotide molecules having sequence regions consisting of contiguous nucleotide stretches of 10-14, 15-20, 30, 50, or even of 100-200 nucleotides or so (including intermediate lengths as well), identical or complementary to a polynucleotide sequence disclosed herein, are particularly contemplated as hybridization probes for use in, e.g., Southern and Northern blotting. This would allow a gene product, or fragment thereof, to be analyzed, both in diverse cell types and also in various bacterial cells. The total size of fragment, as well as the size of the complementary stretch(es), will ultimately depend on the intended use or application of the particular nucleic acid segment. Smaller fragments will generally find use in hybridization embodiments, wherein the length of the contiguous complementary region may be varied, such as between about 15 and about 100 nucleotides, but larger contiguous complementarity stretches may be used, according to the length complementary sequences one wishes to detect.

[0484] The use of a hybridization probe of about 15-25 nucleotides in length allows the formation of a duplex molecule that is both stable and selective. Molecules having contiguous complementary sequences over stretches greater than 15 bases in length are generally preferred, though, in order to increase stability and selectivity of the hybrid, and thereby improve the quality and degree of specific hybrid molecules obtained. One will generally prefer to design nucleic acid molecules having gene-complementary stretches of 15 to 25 contiguous nucleotides, or even longer where desired.

[0485] Hybridization probes may be selected from any portion of any of the sequences disclosed herein. All that is required is to review the sequences set forth herein, or to any continuous portion of the sequences, from about 15-25 nucleotides in length up to and including the full length sequence, that one wishes to utilize as a probe or primer. The choice of probe and primer sequences may be governed by various factors. For example, one may wish to employ primers from towards the termini of the total sequence.

[0486] Small polynucleotide segments or fragments may be readily prepared by, for example, directly synthesizing the fragment by chemical means, as is commonly practiced using an automated oligonucleotide synthesizer. Also, fragments may be obtained by application of nucleic acid reproduction technology, such as the PCR™ technology of U.S. Pat. No. 4,683,202 (incorporated herein by reference), by introducing selected sequences into recombinant vectors for recombinant production, and by other recombinant DNA techniques generally known to those of skill in the art of molecular biology.

[0487] The nucleotide sequences of the invention may be used for their ability to selectively form duplex molecules with complementary stretches of the entire gene or gene fragments of interest. Depending on the application envisioned, one will typically desire to employ varying conditions of hybridization to achieve varying degrees of selectivity of probe towards target sequence. For applications requiring high selectivity, one will typically desire to employ relatively stringent conditions to form the hybrids, e.g., one will select relatively low salt and/or high temperature conditions, such as provided by a salt concentration of from about 0.02 M to about 0.15 M salt at temperatures of from about 50° C. to about 70° C. Such selective conditions tolerate little, if any, mismatch between the probe and the template or target strand, and would be particularly suitable for isolating related sequences.

[0488] Of course, for some applications, for example, where one desires to prepare mutants employing a mutant primer strand hybridized to an underlying template, less stringent (reduced stringency) hybridization conditions will typically be needed in order to allow formation of the heteroduplex. In these circumstances, one may desire to employ salt conditions such as those of from about 0.15 M to about 0.9 M salt, at temperatures ranging from about 20° C. to about 55° C. Cross-hybridizing species can thereby be readily identified as positively hybridizing signals with respect to control hybridizations. In any case, it is generally appreciated that conditions can be rendered more stringent by the addition of increasing amounts of formamide, which serves to destabilize the hybrid duplex in the same manner as increased temperature. Thus, hybridization conditions can be readily manipulated, and thus will generally be a method of choice depending on the desired results.

[0489] According to another embodiment of the present invention, polynucleotide compositions comprising antisense oligonucleotides are provided. Antisense oligonucleotides have been demonstrated to be effective and targeted inhibitors of protein synthesis, and, consequently, provide a therapeutic approach by which a disease can be treated by inhibiting the synthesis of proteins that contribute to the disease. The efficacy of antisense oligonucleotides for inhibiting protein synthesis is well established. For example, the synthesis of polygalactauronase and the muscarine type 2 acetylcholine receptor are inhibited by antisense oligonucleotides directed to their respective mRNA sequences (U.S. Pat. No. 5,739,119 and U.S. Pat. No. 5,759,829). Further, examples of antisense inhibition have been demonstrated with the nuclear protein cyclin, the multiple drug resistance gene (MDG1), ICAM-1, E-selectin, STK-1, striatal GABA_(A) receptor and human EGF (Jaskulski et al., Science. 1988 June 10;240(4858):1544-6; Vasanthakumar and Ahmed, Cancer Commun. 1989;1(4):225-32; Peris et al., Brain Res Mol Brain Res. 1998 June 15;57(2):310-20; U.S. Pat. No. 5,801,154; U.S. Pat. No. 5,789,573; U.S. Pat. No. 5,718,709 and U.S. Pat. No. 5,610,288). Antisense constructs have also been described that inhibit and can be used to treat a variety of abnormal cellular proliferations, e.g., cancer (U.S. Pat. No. 5,747,470; U.S. Pat. No. 5,591,317 and U.S. Pat. No. 5,783,683).

[0490] Therefore, in certain embodiments, the present invention provides oligonucleotide sequences that comprise all, or a portion of, any sequence that is capable of specifically binding to polynucleotide sequence described herein, or a complement thereof. In one embodiment, the antisense oligonucleotides comprise DNA or derivatives thereof. In another embodiment, the oligonucleotides comprise RNA or derivatives thereof. In a third embodiment, the oligonucleotides are modified DNAs comprising a phosphorothioated modified backbone. In a fourth embodiment, the oligonucleotide sequences comprise peptide nucleic acids or derivatives thereof. In each case, preferred compositions comprise a sequence region that is complementary, and more preferably substantially-complementary, and even more preferably, completely complementary to one or more portions of polynucleotides disclosed herein. Selection of antisense compositions specific for a given gene sequence is based upon analysis of the chosen target sequence and determination of secondary structure, T_(m), binding energy, and relative stability. Antisense compositions may be selected based upon their relative inability to form dimers, hairpins, or other secondary structures that would reduce or prohibit specific binding to the target mRNA in a host cell. Highly preferred target regions of the mRNA, are those which are at or near the AUG translation initiation codon, and those sequences which are substantially complementary to 5′ regions of the mRNA. These secondary structure analyses and target site selection considerations can be performed, for example, using v.4 of the OLIGO primer analysis software and/or the BLASTN 2.0.5 algorithm software (Altschul et al., Nucleic Acids Res. 1997, 25(17):3389-402).

[0491] The use of an antisense delivery method employing a short peptide vector, termed MPG (27 residues), is also contemplated. The MPG peptide contains a hydrophobic domain derived from the fusion sequence of HIV gp41 and a hydrophilic domain from the nuclear localization sequence of SV40 T-antigen (Morris et al., Nucleic Acids Res. 1997 July 15;25(14):2730-6). It has been demonstrated that several molecules of the MPG peptide coat the antisense oligonucleotides and can be delivered into cultured mammalian cells in less than 1 hour with relatively high efficiency (90%). Further, the interaction with MPG strongly increases both the stability of the oligonucleotide to nuclease and the ability to cross the plasma membrane.

[0492] According to another embodiment of the invention, the polynucleotide compositions described herein are used in the design and preparation of ribozyme molecules for inhibiting expression of the tumor polypeptides and proteins of the present invention in tumor cells. Ribozymes are RNA-protein complexes that cleave nucleic acids in a site-specific fashion. Ribozymes have specific catalytic domains that possess endonuclease activity (Kim and Cech, Proc Natl Acad Sci USA. 1987 December;84(24):8788-92; Forster and Symons, Cell. 1987 April 24;49(2):211-20). For example, a large number of ribozymes accelerate phosphoester transfer reactions with a high degree of specificity, often cleaving only one of several phosphoesters in an oligonucleotide substrate (Cech et al., Cell. 1981 December; 27(3 Pt 2):487-96; Michel and Westhof, J Mol Biol. 1990 December 5;216(3):585-610; Reinhold-Hurek and Shub, Nature. 1992 May 14;357(6374):173-6). This specificity has been attributed to the requirement that the substrate bind via specific base-pairing interactions to the internal guide sequence (“IGS”) of the ribozyme prior to chemical reaction.

[0493] Six basic varieties of naturally-occurring enzymatic RNAs are known presently. Each can catalyze the hydrolysis of RNA phosphodiester bonds in trans (and thus can cleave other RNA molecules) under physiological conditions. In general, enzymatic nucleic acids act by first binding to a target RNA. Such binding occurs through the target binding portion of a enzymatic nucleic acid which is held in close proximity to an enzymatic portion of the molecule that acts to cleave the target RNA. Thus, the enzymatic nucleic acid first recognizes and then binds a target RNA through complementary base-pairing, and once bound to the correct site, acts enzymatically to cut the target RNA. Strategic cleavage of such a target RNA will destroy its ability to direct synthesis of an encoded protein. After an enzymatic nucleic acid has bound and cleaved its RNA target, it is released from that RNA to search for another target and can repeatedly bind and cleave new targets.

[0494] The enzymatic nature of a ribozyme is advantageous over many technologies, such as antisense technology (where a nucleic acid molecule simply binds to a nucleic acid target to block its translation) since the concentration of ribozyme necessary to affect a therapeutic treatment is lower than that of an antisense oligonucleotide. This advantage reflects the ability of the ribozyme to act enzymatically. Thus, a single ribozyme molecule is able to cleave many molecules of target RNA. In addition, the ribozyme is a highly specific inhibitor, with the specificity of inhibition depending not only on the base pairing mechanism of binding to the target RNA, but also on the mechanism of target RNA cleavage. Single mismatches, or base-substitutions, near the site of cleavage can completely eliminate catalytic activity of a ribozyme. Similar mismatches in antisense molecules do not prevent their action (Woolf et al., Proc Natl Acad Sci USA. 1992 August 15;89(16):7305-9). Thus, the specificity of action of a ribozyme is greater than that of an antisense oligonucleotide binding the same RNA site.

[0495] The enzymatic nucleic acid molecule may be formed in a hammerhead, hairpin, a hepatitis δ virus, group I intron or RNaseP RNA (in association with an RNA guide sequence) or Neurospora VS RNA motif. Examples of hammerhead motifs are described by Rossi et al. Nucleic Acids Res. 1992 September 11;20(17):4559-65. Examples of hairpin motifs are described by Hampel et al. (Eur. Pat. Appl. Publ. No. EP 0360257), Hampel and Tritz, Biochemistry 1989 June 13;28(12):4929-33; Hampel et al., Nucleic Acids Res. 1990 January 25;18(2):299-304 and U.S. Pat. No. 5,631,359. An example of the hepatitis δ virus motif is described by Perrotta and Been, Biochemistry. 1992 December 1;31(47):11843-52; an example of the RNaseP motif is described by Guerrier-Takada et al., Cell. 1983 December; 35(3 Pt 2):849-57; Neurospora VS RNA ribozyme motif is described by Collins (Saville and Collins, Cell. 1990 May 18;61(4):685-96; Saville and Collins, Proc Natl Acad Sci USA. 1991 October 1;88(19):8826-30; Collins and Olive, Biochemistry. 1993 March 23; 32(11):2795-9); and an example of the Group I intron is described in (U.S. Pat. No. 4,987,071). All that is important in an enzymatic nucleic acid molecule of this invention is that it has a specific substrate binding site which is complementary to one or more of the target gene RNA regions, and that it have nucleotide sequences within or surrounding that substrate binding site which impart an RNA cleaving activity to the molecule. Thus the ribozyme constructs need not be limited to specific motifs mentioned herein.

[0496] Ribozymes may be designed as described in Int. Pat. Appl. Publ. No. WO 93/23569 and Int. Pat. Appl. Publ. No. WO 94/02595, each specifically incorporated herein by reference) and synthesized to be tested in vitro and in vivo, as described. Such ribozymes can also be optimized for delivery. While specific examples are provided, those in the art will recognize that equivalent RNA targets in other species can be utilized when necessary.

[0497] Ribozyme activity can be optimized by altering the length of the ribozyme binding arms, or chemically synthesizing ribozymes with modifications that prevent their degradation by serum ribonucleases (see e.g., Int. Pat. Appl. Publ. No. WO 92/07065; Int. Pat. Appl. Publ. No. WO 93/15187; Int. Pat. Appl. Publ. No. WO 91/03162; Eur. Pat. Appl. Publ. No. 92110298.4; U.S. Pat. No. 5,334,711; and Int. Pat. Appl. Publ. No. WO 94/13688, which describe various chemical modifications that can be made to the sugar moieties of enzymatic RNA molecules), modifications which enhance their efficacy in cells, and removal of stem II bases to shorten RNA synthesis times and reduce chemical requirements.

[0498] Sullivan et al. (Int. Pat. Appl. Publ. No. WO 94/02595) describes the general methods for delivery of enzymatic RNA molecules. Ribozymes may be administered to cells by a variety of methods known to those familiar to the art, including, but not restricted to, encapsulation in liposomes, by iontophoresis, or by incorporation into other vehicles, such as hydrogels, cyclodextrins, biodegradable nanocapsules, and bioadhesive microspheres. For some indications, ribozymes may be directly delivered ex vivo to cells or tissues with or without the aforementioned vehicles. Alternatively, the RNA/vehicle combination may be locally delivered by direct inhalation, by direct injection or by use of a catheter, infusion pump or stent. Other routes of delivery include, but are not limited to, intravascular, intramuscular, subcutaneous or joint injection, aerosol inhalation, oral (tablet or pill form), topical, systemic, ocular, intraperitoneal and/or intrathecal delivery. More detailed descriptions of ribozyme delivery and administration are provided in Int. Pat. Appl. Publ. No. WO 94/02595 and Int. Pat. Appl. Publ. No. WO 93/23569, each specifically incorporated herein by reference.

[0499] Another means of accumulating high concentrations of a ribozyme(s) within cells is to incorporate the ribozyme-encoding sequences into a DNA expression vector. Transcription of the ribozyme sequences are driven from a promoter for eukaryotic RNA polymerase I (pol I), RNA polymerase II (pol II), or RNA polymerase III (pol III). Transcripts from pol II or pol III promoters will be expressed at high levels in all cells; the levels of a given pol II promoter in a given cell type will depend on the nature of the gene regulatory sequences (enhancers, silencers, etc.) present nearby. Prokaryotic RNA polymerase promoters may also be used, providing that the prokaryotic RNA polymerase enzyme is expressed in the appropriate cells Ribozymes expressed from such promoters have been shown to function in mammalian cells. Such transcription units can be incorporated into a variety of vectors for introduction into mammalian cells, including but not restricted to, plasmid DNA vectors, viral DNA vectors (such as adenovirus or adeno-associated vectors), or viral RNA vectors (such as retroviral, semliki forest virus, sindbis virus vectors).

[0500] In another embodiment of the invention, peptide nucleic acids (PNAs) compositions are provided. PNA is a DNA mimic in which the nucleobases are attached to a pseudopeptide backbone (Good and Nielsen, Antisense Nucleic Acid Drug Dev. 1997 7(4) 431-37). PNA is able to be utilized in a number methods that traditionally have used RNA or DNA. Often PNA sequences perform better in techniques than the corresponding RNA or DNA sequences and have utilities that are not inherent to RNA or DNA. A review of PNA including methods of making, characteristics of, and methods of using, is provided by Corey (Trends Biotechnol 1997 June; 15(6):224-9). As such, in certain embodiments, one may prepare PNA sequences that are complementary to one or more portions of the ACE mRNA sequence, and such PNA compositions may be used to regulate, alter, decrease, or reduce the translation of ACE-specific mRNA, and thereby alter the level of ACE activity in a host cell to which such PNA compositions have been administered.

[0501] PNAs have 2-aminoethyl-glycine linkages replacing the normal phosphodiester backbone of DNA (Nielsen et al., Science 1991 December 6; 254(5037):1497-500; Hanvey et al., Science. 1992 November 27;258(5087):1481-5; Hyrup and Nielsen, Bioorg Med Chem. 1996 January; 4(1):5-23). This chemistry has three important consequences: firstly, in contrast to DNA or phosphorothioate oligonucleotides, PNAs are neutral molecules; secondly, PNAs are achiral, which avoids the need to develop a stereoselective synthesis; and thirdly, PNA synthesis uses standard Boc or Fmoc protocols for solid-phase peptide synthesis, although other methods, including a modified Merrifield method, have been used.

[0502] PNA monomers or ready-made oligomers are commercially available from PerSeptive Biosystems (Framingham, Mass.). PNA syntheses by either Boc or Fmoc protocols are straightforward using manual or automated protocols (Norton et al., Bioorg Med Chem. 1995 April; 3(4):437-45). The manual protocol lends itself to the production of chemically modified PNAs or the simultaneous synthesis of families of closely related PNAs.

[0503] As with peptide synthesis, the success of a particular PNA synthesis will depend on the properties of the chosen sequence. For example, while in theory PNAs can incorporate any combination of nucleotide bases, the presence of adjacent purines can lead to deletions of one or more residues in the product. In expectation of this difficulty, it is suggested that, in producing PNAs with adjacent purines, one should repeat the coupling of residues likely to be added inefficiently. This should be followed by the purification of PNAs by reverse-phase high-pressure liquid chromatography, providing yields and purity of product similar to those observed during the synthesis of peptides.

[0504] Modifications of PNAs for a given application may be accomplished by coupling amino acids during solid-phase synthesis or by attaching compounds that contain a carboxylic acid group to the exposed N-terminal amine. Alternatively, PNAs can be modified after synthesis by coupling to an introduced lysine or cysteine. The ease with which PNAs can be modified facilitates optimization for better solubility or for specific functional requirements. Once synthesized, the identity of PNAs and their derivatives can be confirmed by mass spectrometry. Several studies have made and utilized modifications of PNAs (for example, Norton et al., Bioorg Med Chem. 1995 April;3(4):437-45; Petersen et al., J Pept Sci. 1995 May-June;1(3):175-83; Orum et al., Biotechniques. 1995 September;19(3):472-80; Footer et al., Biochemistry. 1996 August 20;35(33):10673-9; Griffith et al., Nucleic Acids Res. 1995 August 11;23(15):3003-8; Pardridge et al., Proc Natl Acad Sci USA. 1995 June 6;92(12):5592-6; Boffa et al., Proc Natl Acad Sci USA. 1995 March 14;92(6):1901-5; Gambacorti-Passerini et al., Blood. 1996 August 15;88(4):1411-7; Armitage et al., Proc Natl Acad Sci USA. 1997 November 11;94(23):12320-5; Seeger et al., Biotechniques. 1997 September;23(3):512-7). U.S. Pat. No. 5,700,922 discusses PNA-DNA-PNA chimeric molecules and their uses in diagnostics, modulating protein in organisms, and treatment of conditions susceptible to therapeutics.

[0505] Methods of characterizing the antisense binding properties of PNAs are discussed in Rose (Anal Chem. 1993 December 15;65(24):3545-9) and Jensen et al. (Biochemistry. 1997 April 22;36(16):5072-7). Rose uses capillary gel electrophoresis to determine binding of PNAs to their complementary oligonucleotide, measuring the relative binding kinetics and stoichiometry. Similar types of measurements were made by Jensen et al. using BIAcore™ technology.

[0506] Other applications of PNAs that have been described and will be apparent to the skilled artisan include use in DNA strand invasion, antisense inhibition, mutational analysis, enhancers of transcription, nucleic acid purification, isolation of transcriptionally active genes, blocking of transcription factor binding, genome cleavage, biosensors, in situ hybridization, and the like.

[0507] Polynucleotide Identification, Characterization and Expression

[0508] Polynucleotides compositions of the present invention may be identified, prepared and/or manipulated using any of a variety of well established techniques (see generally, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1989, and other like references). For example, a polynucleotide may be identified, as described in more detail below, by screening a microarray of cDNAs for tumor-associated expression (i.e., expression that is at least two fold greater in a tumor than in normal tissue, as determined using a representative assay provided herein). Such screens may be performed, for example, using the microarray technology of Affymetrix, Inc. (Santa Clara, Calif.) according to the manufacturer's instructions (and essentially as described by Schena et al., Proc. Natl. Acad. Sci. USA 93:10614-10619, 1996 and Heller et al., Proc. Natl. Acad. Sci. USA 94:2150-2155, 1997). Alternatively, polynucleotides may be amplified from cDNA prepared from cells expressing the proteins described herein, such as tumor cells.

[0509] Many template dependent processes are available to amplify a target sequences of interest present in a sample. One of the best known amplification methods is the polymerase chain reaction (PCR™) which is described in detail in U.S. Pat. Nos. 4,683,195, 4,683,202 and 4,800,159, each of which is incorporated herein by reference in its entirety. Briefly, in PCR™, two primer sequences are prepared which are complementary to regions on opposite complementary strands of the target sequence. An excess of deoxynucleoside triphosphates is added to a reaction mixture along with a DNA polymerase (e.g., Taq polymerase). If the target sequence is present in a sample, the primers will bind to the target and the polymerase will cause the primers to be extended along the target sequence by adding on nucleotides. By raising and lowering the temperature of the reaction mixture, the extended primers will dissociate from the target to form reaction products, excess primers will bind to the target and to the reaction product and the process is repeated. Preferably reverse transcription and PCR™ amplification procedure may be performed in order to quantify the amount of mRNA amplified. Polymerase chain reaction methodologies are well known in the art.

[0510] Any of a number of other template dependent processes, many of which are variations of the PCR™ amplification technique, are readily known and available in the art. Illustratively, some such methods include the ligase chain reaction (referred to as LCR), described, for example, in Eur. Pat. Appl. Publ. No. 320,308 and U.S. Pat. No. 4,883,750; Qbeta Replicase, described in PCT Intl. Pat. Appl. Publ. No. PCT/US87/00880; Strand Displacement Amplification (SDA) and Repair Chain Reaction (RCR). Still other amplification methods are described in Great Britain Pat. Appl. No. 2 202 328, and in PCT Intl. Pat. Appl. Publ. No. PCT/US89/01025. Other nucleic acid amplification procedures include transcription-based amplification systems (TAS) (PCT Intl. Pat. Appl. Publ. No. WO 88/10315), including nucleic acid sequence based amplification (NASBA) and 3SR. Eur. Pat. Appl. Publ. No. 329,822 describes a nucleic acid amplification process involving cyclically synthesizing single-stranded RNA (“ssRNA”), ssDNA, and double-stranded DNA (dsDNA). PCT Intl. Pat. Appl. Publ. No. WO 89/06700 describes a nucleic acid sequence amplification scheme based on the hybridization of a promoter/primer sequence to a target single-stranded DNA (“ssDNA”) followed by transcription of many RNA copies of the sequence. Other amplification methods such as “RACE” (Frohman, 1990), and “one-sided PCR” (Ohara, 1989) are also well-known to those of skill in the art.

[0511] An amplified portion of a polynucleotide of the present invention may be used to isolate a full length gene from a suitable library (e.g., a tumor cDNA library) using well known techniques. Within such techniques, a library (cDNA or genomic) is screened using one or more polynucleotide probes or primers suitable for amplification. Preferably, a library is size-selected to include larger molecules. Random primed libraries may also be preferred for identifying 5′ and upstream regions of genes. Genomic libraries are preferred for obtaining introns and extending 5′ sequences.

[0512] For hybridization techniques, a partial sequence may be labeled (e.g., by nick-translation or end-labeling with ³²P) using well known techniques. A bacterial or bacteriophage library is then generally screened by hybridizing filters containing denatured bacterial colonies (or lawns containing phage plaques) with the labeled probe (see Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1989). Hybridizing colonies or plaques are selected and expanded, and the DNA is isolated for further analysis. cDNA clones may be analyzed to determine the amount of additional sequence by, for example, PCR using a primer from the partial sequence and a primer from the vector. Restriction maps and partial sequences may be generated to identify one or more overlapping clones. The complete sequence may then be determined using standard techniques, which may involve generating a series of deletion clones. The resulting overlapping sequences can then assembled into a single contiguous sequence. A full length cDNA molecule can be generated by ligating suitable fragments, using well known techniques.

[0513] Alternatively, amplification techniques, such as those described above, can be useful for obtaining a full length coding sequence from a partial cDNA sequence. One such amplification technique is inverse PCR (see Triglia et al., Nuc. Acids Res. 16:8186, 1988), which uses restriction enzymes to generate a fragment in the known region of the gene. The fragment is then circularized by intramolecular ligation and used as a template for PCR with divergent primers derived from the known region. Within an alternative approach, sequences adjacent to a partial sequence may be retrieved by amplification with a primer to a linker sequence and a primer specific to a known region. The amplified sequences are typically subjected to a second round of amplification with the same linker primer and a second primer specific to the known region. A variation on this procedure, which employs two primers that initiate extension in opposite directions from the known sequence, is described in WO 96/38591. Another such technique is known as “rapid amplification of cDNA ends” or RACE. This technique involves the use of an internal primer and an external primer, which hybridizes to a polyA region or vector sequence, to identify sequences that are 5′ and 3′ of a known sequence. Additional techniques include capture PCR (Lagerstrom et al., PCR Methods Applic. 1:111-19, 1991) and walking PCR (Parker et al., Nucl. Acids. Res. 19:3055-60, 1991). Other methods employing amplification may also be employed to obtain a full length cDNA sequence.

[0514] In certain instances, it is possible to obtain a full length cDNA sequence by analysis of sequences provided in an expressed sequence tag (EST) database, such as that available from GenBank. Searches for overlapping ESTs may generally be performed using well known programs (e.g., NCBI BLAST searches), and such ESTs may be used to generate a contiguous full length sequence. Full length DNA sequences may also be obtained by analysis of genomic fragments.

[0515] In other embodiments of the invention, polynucleotide sequences or fragments thereof which encode polypeptides of the invention, or fusion proteins or functional equivalents thereof, may be used in recombinant DNA molecules to direct expression of a polypeptide in appropriate host cells. Due to the inherent degeneracy of the genetic code, other DNA sequences that encode substantially the same or a functionally equivalent amino acid sequence may be produced and these sequences may be used to clone and express a given polypeptide.

[0516] As will be understood by those of skill in the art, it may be advantageous in some instances to produce polypeptide-encoding nucleotide sequences possessing non-naturally occurring codons. For example, codons preferred by a particular prokaryotic or eukaryotic host can be selected to increase the rate of protein expression or to produce a recombinant RNA transcript having desirable properties, such as a half-life which is longer than that of a transcript generated from the naturally occurring sequence.

[0517] Moreover, the polynucleotide sequences of the present invention can be engineered using methods generally known in the art in order to alter polypeptide encoding sequences for a variety of reasons, including but not limited to, alterations which modify the cloning, processing, and/or expression of the gene product. For example, DNA shuffling by random fragmentation and PCR reassembly of gene fragments and synthetic oligonucleotides may be used to engineer the nucleotide sequences. In addition, site-directed mutagenesis may be used to insert new restriction sites, alter glycosylation patterns, change codon preference, produce splice variants, or introduce mutations, and so forth.

[0518] In another embodiment of the invention, natural, modified, or recombinant nucleic acid sequences may be ligated to a heterologous sequence to encode a fusion protein. For example, to screen peptide libraries for inhibitors of polypeptide activity, it may be useful to encode a chimeric protein that can be recognized by a commercially available antibody. A fusion protein may also be engineered to contain a cleavage site located between the polypeptide-encoding sequence and the heterologous protein sequence, so that the polypeptide may be cleaved and purified away from the heterologous moiety.

[0519] Sequences encoding a desired polypeptide may be synthesized, in whole or in part, using chemical methods well known in the art (see Caruthers, M. H. et al. (1980) Nucl. Acids Res. Symp. Ser. 215-223, Horn, T. et al. (1980) Nucl. Acids Res. Symp. Ser. 225-232). Alternatively, the protein itself may be produced using chemical methods to synthesize the amino acid sequence of a polypeptide, or a portion thereof. For example, peptide synthesis can be performed using various solid-phase techniques (Roberge, J. Y. et al. (1995) Science 269:202-204) and automated synthesis may be achieved, for example, using the ABI 431 A Peptide Synthesizer (Perkin Elmer, Palo Alto, Calif.).

[0520] A newly synthesized peptide may be substantially purified by preparative high performance liquid chromatography (e.g., Creighton, T. (1983) Proteins, Structures and Molecular Principles, W H Freeman and Co., New York, N.Y.) or other comparable techniques available in the art. The composition of the synthetic peptides may be confirmed by amino acid analysis or sequencing (e.g., the Edman degradation procedure). Additionally, the amino acid sequence of a polypeptide, or any part thereof, may be altered during direct synthesis and/or combined using chemical methods with sequences from other proteins, or any part thereof, to produce a variant polypeptide.

[0521] In order to express a desired polypeptide, the nucleotide sequences encoding the polypeptide, or functional equivalents, may be inserted into appropriate expression vector, i.e., a vector which contains the necessary elements for the transcription and translation of the inserted coding sequence. Methods which are well known to those skilled in the art may be used to construct expression vectors containing sequences encoding a polypeptide of interest and appropriate transcriptional and translational control elements. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. Such techniques are described, for example, in Sambrook, J. et al. (1989) Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y., and Ausubel, F. M. et al. (1989) Current Protocols in Molecular Biology, John Wiley & Sons, New York. N.Y.

[0522] A variety of expression vector/host systems may be utilized to contain and express polynucleotide sequences. These include, but are not limited to, microorganisms such as bacteria transformed with recombinant bacteriophage, plasmid, or cosmid DNA expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with virus expression vectors (e.g., baculovirus); plant cell systems transformed with virus expression vectors (e.g., cauliflower mosaic virus, CaMV; tobacco mosaic virus, TMV) or with bacterial expression vectors (e.g., Ti or pBR322 plasmids); or animal cell systems.

[0523] The “control elements” or “regulatory sequences” present in an expression vector are those non-translated regions of the vector—enhancers, promoters, 5′ and 3′ untranslated regions—which interact with host cellular proteins to carry out transcription and translation. Such elements may vary in their strength and specificity. Depending on the vector system and host utilized, any number of suitable transcription and translation elements, including constitutive and inducible promoters, may be used. For example, when cloning in bacterial systems, inducible promoters such as the hybrid lacZ promoter of the PBLUESCRIPT phagemid (Stratagene, La Jolla, Calif.) or PSPORT1 plasmid (Gibco BRL, Gaithersburg, Md.) and the like may be used. In mammalian cell systems, promoters from mammalian genes or from mammalian viruses are generally preferred. If it is necessary to generate a cell line that contains multiple copies of the sequence encoding a polypeptide, vectors based on SV40 or EBV may be advantageously used with an appropriate selectable marker.

[0524] In bacterial systems, any of a number of expression vectors may be selected depending upon the use intended for the expressed polypeptide. For example, when large quantities are needed, for example for the induction of antibodies, vectors which direct high level expression of fusion proteins that are readily purified may be used. Such vectors include, but are not limited to, the multifunctional E. coli cloning and expression vectors such as BLUESCRIPT (Stratagene), in which the sequence encoding the polypeptide of interest may be ligated into the vector in frame with sequences for the amino-terminal Met and the subsequent 7 residues of .beta.-galactosidase so that a hybrid protein is produced; pIN vectors (Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509); and the like. pGEX Vectors (Promega, Madison, Wis.) may also be used to express foreign polypeptides as fusion proteins with glutathione S-transferase (GST). In general, such fusion proteins are soluble and can easily be purified from lysed cells by adsorption to glutathione-agarose beads followed by elution in the presence of free glutathione. Proteins made in such systems may be designed to include heparin, thrombin, or factor XA protease cleavage sites so that the cloned polypeptide of interest can be released from the GST moiety at will.

[0525] In the yeast, Saccharomyces cerevisiae, a number of vectors containing constitutive or inducible promoters such as alpha factor, alcohol oxidase, and PGH may be used. For reviews, see Ausubel et al. (supra) and Grant et al. (1987) Methods Enzymol. 153:516-544.

[0526] In cases where plant expression vectors are used, the expression of sequences encoding polypeptides may be driven by any of a number of promoters. For example, viral promoters such as the 35S and 19S promoters of CaMV may be used alone or in combination with the omega leader sequence from TMV (Takamatsu, N. (1987) EMBO J. 6:307-311. Alternatively, plant promoters such as the small subunit of RUBISCO or heat shock promoters may be used (Coruzzi, G. et al. (1984) EMBO J. 3:1671-1680; Broglie, R. et al. (1984) Science 224:838-843; and Winter, J. et al. (1991) Results Probl. Cell Differ. 17:85-105). These constructs can be introduced into plant cells by direct DNA transformation or pathogen-mediated transfection. Such techniques are described in a number of generally available reviews (see, for example, Hobbs, S. or Murry, L. E. in McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York, N.Y.; pp. 191-196).

[0527] An insect system may also be used to express a polypeptide of interest. For example, in one such system, Autographa californica nuclear polyhedrosis virus (AcNPV) is used as a vector to express foreign genes in Spodoptera frugiperda cells or in Trichoplusia larvae. The sequences encoding the polypeptide may be cloned into a non-essential region of the virus, such as the polyhedrin gene, and placed under control of the polyhedrin promoter. Successful insertion of the polypeptide-encoding sequence will render the polyhedrin gene inactive and produce recombinant virus lacking coat protein. The recombinant viruses may then be used to infect, for example, S. frugiperda cells or Trichoplusia larvae in which the polypeptide of interest may be expressed (Engelhard, E. K. et al. (1994) Proc. Natl. Acad. Sci. 91:3224-3227).

[0528] In mammalian host cells, a number of viral-based expression systems are generally available. For example, in cases where an adenovirus is used as an expression vector, sequences encoding a polypeptide of interest may be ligated into an adenovirus transcription/translation complex consisting of the late promoter and tripartite leader sequence. Insertion in a non-essential E1 or E3 region of the viral genome may be used to obtain a viable virus which is capable of expressing the polypeptide in infected host cells (Logan, J. and Shenk, T. (1984) Proc. Natl. Acad. Sci. 81:3655-3659). In addition, transcription enhancers, such as the Rous sarcoma virus (RSV) enhancer, may be used to increase expression in mammalian host cells.

[0529] Specific initiation signals may also be used to achieve more efficient translation of sequences encoding a polypeptide of interest. Such signals include the ATG initiation codon and adjacent sequences. In cases where sequences encoding the polypeptide, its initiation codon, and upstream sequences are inserted into the appropriate expression vector, no additional transcriptional or translational control signals may be needed. However, in cases where only coding sequence, or a portion thereof, is inserted, exogenous translational control signals including the ATG initiation codon should be provided. Furthermore, the initiation codon should be in the correct reading frame to ensure translation of the entire insert. Exogenous translational elements and initiation codons may be of various origins, both natural and synthetic. The efficiency of expression may be enhanced by the inclusion of enhancers which are appropriate for the particular cell system which is used, such as those described in the literature (Scharf, D. et al. (1994) Results Probl. Cell Differ. 20:125-162).

[0530] In addition, a host cell strain may be chosen for its ability to modulate the expression of the inserted sequences or to process the expressed protein in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, carboxylation. glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” form of the protein may also be used to facilitate correct insertion, folding and/or function. Different host cells such as CHO, COS, HeLa, MDCK, HEK293, and WI38, which have specific cellular machinery and characteristic mechanisms for such post-translational activities, may be chosen to ensure the correct modification and processing of the foreign protein.

[0531] For long-term, high-yield production of recombinant proteins, stable expression is generally preferred. For example, cell lines which stably express a polynucleotide of interest may be transformed using expression vectors which may contain viral origins of replication and/or endogenous expression elements and a selectable marker gene on the same or on a separate vector. Following the introduction of the vector, cells may be allowed to grow for 1-2 days in an enriched media before they are switched to selective media. The purpose of the selectable marker is to confer resistance to selection, and its presence allows growth and recovery of cells which successfully express the introduced sequences. Resistant clones of stably transformed cells may be proliferated using tissue culture techniques appropriate to the cell type.

[0532] Any number of selection systems may be used to recover transformed cell lines. These include, but are not limited to, the herpes simplex virus thymidine kinase (Wigler, M. et al. (1977) Cell 11:223-32) and adenine phosphoribosyltransferase (Lowy, I. et al. (1990) Cell 22:817-23) genes which can be employed in tk.sup.- or aprt.sup.-cells, respectively. Also, antimetabolite, antibiotic or herbicide resistance can be used as the basis for selection; for example, dhfr which confers resistance to methotrexate (Wigler, M. et al. (1980) Proc. Natl. Acad. Sci. 77:3567-70); npt, which confers resistance to the aminoglycosides, neomycin and G-418 (Colbere-Garapin, F. et al (1981) J. Mol. Biol. 150:1-14); and als or pat, which confer resistance to chlorsulfuron and phosphinotricin acetyltransferase, respectively (Murry, supra). Additional selectable genes have been described, for example, trpB, which allows cells to utilize indole in place of tryptophan, or hisD, which allows cells to utilize histinol in place of histidine (Hartman, S. C. and R. C. Mulligan (1988) Proc. Natl. Acad. Sci. 85:8047-51). The use of visible markers has gained popularity with such markers as anthocyanins, beta-glucuronidase and its substrate GUS, and luciferase and its substrate luciferin, being widely used not only to identify transformants, but also to quantify the amount of transient or stable protein expression attributable to a specific vector system (Rhodes, C. A. et al. (1995) Methods Mol. Biol. 55:121-131).

[0533] Although the presence/absence of marker gene expression suggests that the gene of interest is also present, its presence and expression may need to be confirmed. For example, if the sequence encoding a polypeptide is inserted within a marker gene sequence, recombinant cells containing sequences can be identified by the absence of marker gene function. Alternatively, a marker gene can be placed in tandem with a polypeptide-encoding sequence under the control of a single promoter. Expression of the marker gene in response to induction or selection usually indicates expression of the tandem gene as well.

[0534] Alternatively, host cells that contain and express a desired polynucleotide sequence may be identified by a variety of procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations and protein bioassay or immunoassay techniques which include, for example, membrane, solution, or chip based technologies for the detection and/or quantification of nucleic acid or protein.

[0535] A variety of protocols for detecting and measuring the expression of polynucleotide-encoded products, using either polyclonal or monoclonal antibodies specific for the product are known in the art. Examples include enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), and fluorescence activated cell sorting (FACS). A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering epitopes on a given polypeptide may be preferred for some applications, but a competitive binding assay may also be employed. These and other assays are described, among other places, in Hampton, R. et al. (1990; Serological Methods, a Laboratory Manual, APS Press, St Paul. Minn.) and Maddox, D. E. et al. (1983; J. Exp. Med. 158:1211-1216).

[0536] A wide variety of labels and conjugation techniques are known by those skilled in the art and may be used in various nucleic acid and amino acid assays. Means for producing labeled hybridization or PCR probes for detecting sequences related to polynucleotides include oligolabeling, nick translation, end-labeling or PCR amplification using a labeled nucleotide. Alternatively, the sequences, or any portions thereof may be cloned into a vector for the production of an mRNA probe. Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by addition of an appropriate RNA polymerase such as T7, T3, or SP6 and labeled nucleotides. These procedures may be conducted using a variety of commercially available kits. Suitable reporter molecules or labels, which may be used include radionuclides, enzymes, fluorescent, chemiluminescent, or chromogenic agents as well as substrates, cofactors, inhibitors, magnetic particles, and the like.

[0537] Host cells transformed with a polynucleotide sequence of interest may be cultured under conditions suitable for the expression and recovery of the protein from cell culture. The protein produced by a recombinant cell may be secreted or contained intracellularly depending on the sequence and/or the vector used. As will be understood by those of skill in the art, expression vectors containing polynucleotides of the invention may be designed to contain signal sequences which direct secretion of the encoded polypeptide through a prokaryotic or eukaryotic cell membrane. Other recombinant constructions may be used to join sequences encoding a polypeptide of interest to nucleotide sequence encoding a polypeptide domain which will facilitate purification of soluble proteins. Such purification facilitating domains include, but are not limited to, metal chelating peptides such as histidine-tryptophan modules that allow purification on immobilized metals, protein A domains that allow purification on immobilized immunoglobulin, and the domain utilized in the FLAGS extension/affinity purification system (Immunex Corp., Seattle, Wash.). The inclusion of cleavable linker sequences such as those specific for Factor XA or enterokinase (Invitrogen. San Diego, Calif.) between the purification domain and the encoded polypeptide may be used to facilitate purification. One such expression vector provides for expression of a fusion protein containing a polypeptide of interest and a nucleic acid encoding 6 histidine residues preceding a thioredoxin or an enterokinase cleavage site. The histidine residues facilitate purification on IMIAC (immobilized metal ion affinity chromatography) as described in Porath, J. et al. (1992, Prot. Exp. Purif. 3:263-281) while the enterokinase cleavage site provides a means for purifying the desired polypeptide from the fusion protein. A discussion of vectors which contain fusion proteins is provided in Kroll, D. J. et al. (1993; DNA Cell Biol. 12:441-453).

[0538] In addition to recombinant production methods, polypeptides of the invention, and fragments thereof, may be produced by direct peptide synthesis using solid-phase techniques (Merrifield J. (1963) J. Am. Chem. Soc. 85:2149-2154). Protein synthesis may be performed using manual techniques or by automation. Automated synthesis may be achieved, for example, using Applied Biosystems 431A Peptide Synthesizer (Perkin Elmer). Alternatively, various fragments may be chemically synthesized separately and combined using chemical methods to produce the full length molecule.

[0539] Antibody Compositions, Fragments Thereof and Other Binding Agents

[0540] According to another aspect, the present invention further provides binding agents, such as antibodies and antigen-binding fragments thereof, that exhibit immunological binding to a tumor polypeptide disclosed herein, or to a portion, variant or derivative thereof. An antibody, or antigen-binding fragment thereof, is said to “specifically bind,” “immunogically bind,” and/or is “immunologically reactive” to a polypeptide of the invention if it reacts at a detectable level (within, for example, an ELISA assay) with the polypeptide, and does not react detectably with unrelated polypeptides under similar conditions.

[0541] Immunological binding, as used in this context, generally refers to the non-covalent interactions of the type which occur between an immunoglobulin molecule and an antigen for which the immunoglobulin is specific. The strength, or affinity of immunological binding interactions can be expressed in terms of the dissociation constant (K_(d)) of the interaction, wherein a smaller K_(d) represents a greater affinity. Immunological binding properties of selected polypeptides can be quantified using methods well known in the art. One such method entails measuring the rates of antigen-binding site/antigen complex formation and dissociation, wherein those rates depend on the concentrations of the complex partners, the affinity of the interaction, and on geometric parameters that equally influence the rate in both directions. Thus, both the “on rate constant” (K_(on)) and the “off rate constant” (K_(off)) can be determined by calculation of the concentrations and the actual rates of association and dissociation. The ratio of K_(off)/K_(on) enables cancellation of all parameters not related to affinity, and is thus equal to the dissociation constant K_(d). See, generally, Davies et al. (1990) Annual Rev. Biochem. 59:439-473.

[0542] An “antigen-binding site,” or “binding portion” of an antibody refers to the part of the immunoglobulin molecule that participates in antigen binding. The antigen binding site is formed by amino acid residues of the N-terminal variable (“V”) regions of the heavy (“H”) and light (“L”) chains. Three highly divergent stretches within the V regions of the heavy and light chains are referred to as “hypervariable regions” which are interposed between more conserved flanking stretches known as “framework regions,” or “FRs”. Thus the term “FR” refers to amino acid sequences which are naturally found between and adjacent to hypervariable regions in immunoglobulins. In an antibody molecule, the three hypervariable regions of a light chain and the three hypervariable regions of a heavy chain are disposed relative to each other in three dimensional space to form an antigen-binding surface. The antigen-binding surface is complementary to the three-dimensional surface of a bound antigen, and the three hypervariable regions of each of the heavy and light chains are referred to as “complementarity-determining regions,” or “CDRs.”

[0543] Binding agents may be further capable of differentiating between patients with and without a cancer, such as lung cancer, using the representative assays provided herein. For example, antibodies or other binding agents that bind to a tumor protein will preferably generate a signal indicating the presence of a cancer in at least about 20% of patients with the disease, more preferably at least about 30% of patients. Alternatively, or in addition, the antibody will generate a negative signal indicating the absence of the disease in at least about 90% of individuals without the cancer. To determine whether a binding agent satisfies this requirement, biological samples (e.g., blood, sera, sputum, urine and/or tumor biopsies) from patients with and without a cancer (as determined using standard clinical tests) may be assayed as described herein for the presence of polypeptides that bind to the binding agent. Preferably, a statistically significant number of samples with and without the disease will be assayed. Each binding agent should satisfy the above criteria; however, those of ordinary skill in the art will recognize that binding agents may be used in combination to improve sensitivity.

[0544] Any agent that satisfies the above requirements may be a binding agent. For example, a binding agent may be a ribosome, with or without a peptide component, an RNA molecule or a polypeptide. In a preferred embodiment, a binding agent is an antibody or an antigen-binding fragment thereof. Antibodies may be prepared by any of a variety of techniques known to those of ordinary skill in the art. See, e.g., Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988. In general, antibodies can be produced by cell culture techniques, including the generation of monoclonal antibodies as described herein, or via transfection of antibody genes into suitable bacterial or mammalian cell hosts, in order to allow for the production of recombinant antibodies. In one technique, an immunogen comprising the polypeptide is initially injected into any of a wide variety of mammals (e.g., mice, rats, rabbits, sheep or goats). In this step, the polypeptides of this invention may serve as the immunogen without modification. Alternatively, particularly for relatively short polypeptides, a superior immune response may be elicited if the polypeptide is joined to a carrier protein, such as bovine serum albumin or keyhole limpet hemocyanin. The immunogen is injected into the animal host, preferably according to a predetermined schedule incorporating one or more booster immunizations, and the animals are bled periodically. Polyclonal antibodies specific for the polypeptide may then be purified from such antisera by, for example, affinity chromatography using the polypeptide coupled to a suitable solid support.

[0545] Monoclonal antibodies specific for an antigenic polypeptide of interest may be prepared, for example, using the technique of Kohler and Milstein, Eur. J. Immunol. 6:511-519, 1976, and improvements thereto. Briefly, these methods involve the preparation of immortal cell lines capable of producing antibodies having the desired specificity (i.e., reactivity with the polypeptide of interest). Such cell lines may be produced, for example, from spleen cells obtained from an animal immunized as described above. The spleen cells are then immortalized by, for example, fusion with a myeloma cell fusion partner, preferably one that is syngeneic with the immunized animal. A variety of fusion techniques may be employed. For example, the spleen cells and myeloma cells may be combined with a nonionic detergent for a few minutes and then plated at low density on a selective medium that supports the growth of hybrid cells, but not myeloma cells. A preferred selection technique uses HAT (hypoxanthine, aminopterin, thymidine) selection. After a sufficient time, usually about 1 to 2 weeks, colonies of hybrids are observed. Single colonies are selected and their culture supernatants tested for binding activity against the polypeptide. Hybridomas having high reactivity and specificity are preferred.

[0546] Monoclonal antibodies may be isolated from the supernatants of growing hybridoma colonies. In addition, various techniques may be employed to enhance the yield, such as injection of the hybridoma cell line into the peritoneal cavity of a suitable vertebrate host, such as a mouse. Monoclonal antibodies may then be harvested from the ascites fluid or the blood. Contaminants may be removed from the antibodies by conventional techniques, such as chromatography, gel filtration, precipitation, and extraction. The polypeptides of this invention may be used in the purification process in, for example, an affinity chromatography step.

[0547] A number of therapeutically useful molecules are known in the art which comprise antigen-binding sites that are capable of exhibiting immunological binding properties of an antibody molecule. The proteolytic enzyme papain preferentially cleaves IgG molecules to yield several fragments, two of which (the “F(ab)” fragments) each comprise a covalent heterodimer that includes an intact antigen-binding site. The enzyme pepsin is able to cleave IgG molecules to provide several fragments, including the “F(ab′)₂” fragment which comprises both antigen-binding sites. An “Fv” fragment can be produced by preferential proteolytic cleavage of an IgM, and on rare occasions IgG or IgA immunoglobulin molecule. Fv fragments are, however, more commonly derived using recombinant techniques known in the art. The Fv fragment includes a non-covalent V_(H)::V_(L) heterodimer including an antigen-binding site which retains much of the antigen recognition and binding capabilities of the native antibody molecule. Inbar et al. (1972) Proc. Nat. Acad. Sci. USA 69:2659-2662; Hochman et al. (1976) Biochem 15:2706-2710; and Ehrlich et al. (1980) Biochem 19:4091-4096.

[0548] A single chain Fv (“sFv”) polypeptide is a covalently linked V_(H)::V_(L) heterodimer which is expressed from a gene fusion including V_(H)- and V_(L)-encoding genes linked by a peptide-encoding linker. Huston et al. (1988) Proc. Nat. Acad. Sci. USA 85(16):5879-5883. A number of methods have been described to discern chemical structures for converting the naturally aggregated—but chemically separated—light and heavy polypeptide chains from an antibody V region into an sFv molecule which will fold into a three dimensional structure substantially similar to the structure of an antigen-binding site. See, e.g., U.S. Pat. Nos. 5,091,513 and 5,132,405, to Huston et al.; and U.S. Pat. No. 4,946,778, to Ladner et al.

[0549] Each of the above-described molecules includes a heavy chain and a light chain CDR set, respectively interposed between a heavy chain and a light chain FR set which provide support to the CDRS and define the spatial relationship of the CDRs relative to each other. As used herein, the term “CDR set” refers to the three hypervariable regions of a heavy or light chain V region. Proceeding from the N-terminus of a heavy or light chain, these regions are denoted as “CDR1,” “CDR2,” and “CDR3” respectively. An antigen-binding site, therefore, includes six CDRs, comprising the CDR set from each of a heavy and a light chain V region. A polypeptide comprising a single CDR, (e.g., a CDR1, CDR2 or CDR3) is referred to herein as a “molecular recognition unit.” Crystallographic analysis of a number of antigen-antibody complexes has demonstrated that the amino acid residues of CDRs form extensive contact with bound antigen, wherein the most extensive antigen contact is with the heavy chain CDR3. Thus, the molecular recognition units are primarily responsible for the specificity of an antigen-binding site.

[0550] As used herein, the term “FR set” refers to the four flanking amino acid sequences which frame the CDRs of a CDR set of a heavy or light chain V region. Some FR residues may contact bound antigen; however, FRs are primarily responsible for folding the V region into the antigen-binding site, particularly the FR residues directly adjacent to the CDRS. Within FRs, certain amino residues and certain structural features are very highly conserved. In this regard, all V region sequences contain an internal disulfide loop of around 90 amino acid residues. When the V regions fold into a binding-site, the CDRs are displayed as projecting loop motifs which form an antigen-binding surface. It is generally recognized that there are conserved structural regions of FRs which influence the folded shape of the CDR loops into certain “canonical” structures—regardless of the precise CDR amino acid sequence. Further, certain FR residues are known to participate in non-covalent interdomain contacts which stabilize the interaction of the antibody heavy and light chains.

[0551] A number of “humanized” antibody molecules comprising an antigen-binding site derived from a non-human immunoglobulin have been described, including chimeric antibodies having rodent V regions and their associated CDRs fused to human constant domains (Winter et al. (1991) Nature 349:293-299; Lobuglio et al. (1989) Proc. Nat. Acad. Sci. USA 86:4220-4224; Shaw et al. (1987) J Immunol. 138:4534-4538; and Brown et al. (1987) Cancer Res. 47:3577-3583), rodent CDRs grafted into a human supporting FR prior to fusion with an appropriate human antibody constant domain (Riechmann et al. (1988) Nature 332:323-327; Verhoeyen et al. (1988) Science 239:1534-1536; and Jones et al. (1986) Nature 321:522-525), and rodent CDRs supported by recombinantly veneered rodent FRs (European Patent Publication No. 519,596, published Dec. 23, 1992). These “humanized” molecules are designed to minimize unwanted immunological response toward rodent antihuman antibody molecules which limits the duration and effectiveness of therapeutic applications of those moieties in human recipients.

[0552] As used herein, the terms “veneered FRs” and “recombinantly veneered FRs” refer to the selective replacement of FR residues from, e.g., a rodent heavy or light chain V region, with human FR residues in order to provide a xenogeneic molecule comprising an antigen-binding site which retains substantially all of the native FR polypeptide folding structure. Veneering techniques are based on the understanding that the ligand binding characteristics of an antigen-binding site are determined primarily by the structure and relative disposition of the heavy and light chain CDR sets within the antigen-binding surface. Davies et al. (1990) Ann. Rev. Biochem. 59:439-473. Thus, antigen binding specificity can be preserved in a humanized antibody only wherein the CDR structures, their interaction with each other, and their interaction with the rest of the V region domains are carefully maintained. By using veneering techniques, exterior (e.g., solvent-accessible) FR residues which are readily encountered by the immune system are selectively replaced with human residues to provide a hybrid molecule that comprises either a weakly immunogenic, or substantially non-immunogenic veneered surface.

[0553] The process of veneering makes use of the available sequence data for human antibody variable domains compiled by Kabat et al., in Sequences of Proteins of Immunological Interest, 4th ed., (U.S. Dept. of Health and Human Services, U.S. Government Printing Office, 1987), updates to the Kabat database, and other accessible U.S. and foreign databases (both nucleic acid and protein). Solvent accessibilities of V region amino acids can be deduced from the known three-dimensional structure for human and murine antibody fragments. There are two general steps in veneering a murine antigen-binding site. Initially, the FRs of the variable domains of an antibody molecule of interest are compared with corresponding FR sequences of human variable domains obtained from the above-identified sources. The most homologous human V regions are then compared residue by residue to corresponding murine amino acids. The residues in the murine FR which differ from the human counterpart are replaced by the residues present in the human moiety using recombinant techniques well known in the art. Residue switching is only carried out with moieties which are at least partially exposed (solvent accessible), and care is exercised in the replacement of amino acid residues which may have a significant effect on the tertiary structure of V region domains, such as proline, glycine and charged amino acids.

[0554] In this manner, the resultant “veneered” murine antigen-binding sites are thus designed to retain the murine CDR residues, the residues substantially adjacent to the CDRs, the residues identified as buried or mostly buried (solvent inaccessible), the residues believed to participate in non-covalent (e.g., electrostatic and hydrophobic) contacts between heavy and light chain domains, and the residues from conserved structural regions of the FRs which are believed to influence the “canonical” tertiary structures of the CDR loops. These design criteria are then used to prepare recombinant nucleotide sequences which combine the CDRs of both the heavy and light chain of a murine antigen-binding site into human-appearing FRs that can be used to transfect mammalian cells for the expression of recombinant human antibodies which exhibit the antigen specificity of the murine antibody molecule.

[0555] In another embodiment of the invention, monoclonal antibodies of the present invention may be coupled to one or more therapeutic agents. Suitable agents in this regard include radionuclides, differentiation inducers, drugs, toxins, and derivatives thereof. Preferred radionuclides include ⁹⁰Y, ¹²³I, ¹²⁵I, ¹³¹I, ¹⁸⁶Re, ¹⁸⁸Re, ²¹¹AT, and ²¹²Bi. Preferred drugs include methotrexate, and pyrimidine and purine analogs. Preferred differentiation inducers include phorbol esters and butyric acid. Preferred toxins include ricin, abrin, diptheria toxin, cholera toxin, gelonin, Pseudomonas exotoxin, Shigella toxin, and pokeweed antiviral protein.

[0556] A therapeutic agent may be coupled (e.g., covalently bonded) to a suitable monoclonal antibody either directly or indirectly (e.g., via a linker group). A direct reaction between an agent and an antibody is possible when each possesses a substituent capable of reacting with the other. For example, a nucleophilic group, such as an amino or sulfhydryl group, on one may be capable of reacting with a carbonyl-containing group, such as an anhydride or an acid halide, or with an alkyl group containing a good leaving group (e.g., a halide) on the other.

[0557] Alternatively, it may be desirable to couple a therapeutic agent and an antibody via a linker group. A linker group can function as a spacer to distance an antibody from an agent in order to avoid interference with binding capabilities. A linker group can also serve to increase the chemical reactivity of a substituent on an agent or an antibody, and thus increase the coupling efficiency. An increase in chemical reactivity may also facilitate the use of agents, or functional groups on agents, which otherwise would not be possible.

[0558] It will be evident to those skilled in the art that a variety of bifunctional or polyfunctional reagents, both homo- and hetero-functional (such as those described in the catalog of the Pierce Chemical Co., Rockford, Ill.), may be employed as the linker group. Coupling may be effected, for example, through amino groups, carboxyl groups, sulfhydryl groups or oxidized carbohydrate residues. There are numerous references describing such methodology, e.g., U.S. Pat. No. 4,671,958, to Rodwell et al.

[0559] Where a therapeutic agent is more potent when free from the antibody portion of the immunoconjugates of the present invention, it may be desirable to use a linker group which is cleavable during or upon internalization into a cell. A number of different cleavable linker groups have been described. The mechanisms for the intracellular release of an agent from these linker groups include cleavage by reduction of a disulfide bond (e.g., U.S. Pat. No. 4,489,710, to Spitler), by irradiation of a photolabile bond (e.g., U.S. Pat. No. 4,625,014, to Senter et al.), by hydrolysis of derivatized amino acid side chains (e.g., U.S. Pat. No. 4,638,045, to Kohn et al.), by serum complement-mediated hydrolysis (e.g., U.S. Pat. No. 4,671,958, to Rodwell et al.), and acid-catalyzed hydrolysis (e.g., U.S. Pat. No. 4,569,789, to Blattler et al.).

[0560] It may be desirable to couple more than one agent to an antibody. In one embodiment, multiple molecules of an agent are coupled to one antibody molecule. In another embodiment, more than one type of agent may be coupled to one antibody. Regardless of the particular embodiment, immunoconjugates with more than one agent may be prepared in a variety of ways. For example, more than one agent may be coupled directly to an antibody molecule, or linkers that provide multiple sites for attachment can be used. Alternatively, a carrier can be used.

[0561] A carrier may bear the agents in a variety of ways, including covalent bonding either directly or via a linker group. Suitable carriers include proteins such as albumins (e.g., U.S. Pat. No. 4,507,234, to Kato et al.), peptides and polysaccharides such as aminodextran (e.g., U.S. Pat. No. 4,699,784, to Shih et al.). A carrier may also bear an agent by noncovalent bonding or by encapsulation, such as within a liposome vesicle (e.g., U.S. Pat. Nos. 4,429,008 and 4,873,088). Carriers specific for radionuclide agents include radiohalogenated small molecules and chelating compounds. For example, U.S. Pat. No. 4,735,792 discloses representative radiohalogenated small molecules and their synthesis. A radionuclide chelate may be formed from chelating compounds that include those containing nitrogen and sulfur atoms as the donor atoms for binding the metal, or metal oxide, radionuclide. For example, U.S. Pat. No. 4,673,562, to Davison et al. discloses representative chelating compounds and their synthesis.

[0562] T Cell Compositions

[0563] The present invention, in another aspect, provides T cells specific for a tumor polypeptide disclosed herein, or for a variant or derivative thereof. Such cells may generally be prepared in vitro or ex vivo, using standard procedures. For example, T cells may be isolated from bone marrow, peripheral blood, or a fraction of bone marrow or peripheral blood of a patient, using a commercially available cell separation system, such as the Isolex™ System, available from Nexell Therapeutics, Inc. (Irvine, Calif.; see also U.S. Pat. No. 5,240,856; U.S. Pat. No. 5,215,926; WO 89/06280; WO 91/16116 and WO 92/07243). Alternatively, T cells may be derived from related or unrelated humans, non-human mammals, cell lines or cultures.

[0564] T cells may be stimulated with a polypeptide, polynucleotide encoding a polypeptide and/or an antigen presenting cell (APC) that expresses such a polypeptide. Such stimulation is performed under conditions and for a time sufficient to permit the generation of T cells that are specific for the polypeptide of interest. Preferably, a tumor polypeptide or polynucleotide of the invention is present within a delivery vehicle, such as a microsphere, to facilitate the generation of specific T cells.

[0565] T cells are considered to be specific for a polypeptide of the present invention if the T cells specifically proliferate, secrete cytokines or kill target cells coated with the polypeptide or expressing a gene encoding the polypeptide. T cell specificity may be evaluated using any of a variety of standard techniques. For example, within a chromium release assay or proliferation assay, a stimulation index of more than two fold increase in lysis and/or proliferation, compared to negative controls, indicates T cell specificity. Such assays may be performed, for example, as described in Chen et al., Cancer Res. 54:1065-1070, 1994. Alternatively, detection of the proliferation of T cells may be accomplished by a variety of known techniques. For example, T cell proliferation can be detected by measuring an increased rate of DNA synthesis (e.g., by pulse-labeling cultures of T cells with tritiated thymidine and measuring the amount of tritiated thymidine incorporated into DNA). Contact with a tumor polypeptide (100 ng/ml -100 μg/ml, preferably 200 ng/ml-25 μg/ml) for 3-7 days will typically result in at least a two fold increase in proliferation of the T cells. Contact as described above for 2-3 hours should result in activation of the T cells, as measured using standard cytokine assays in which a two fold increase in the level of cytokine release (e.g., TNF or IFN-γ) is indicative of T cell activation (see Coligan et al., Current Protocols in Immunology, vol. 1, Wiley Interscience (Greene 1998)). T cells that have been activated in response to a tumor polypeptide, polynucleotide or polypeptide-expressing APC may be CD4⁺ and/or CD8⁺. Tumor polypeptide-specific T cells may be expanded using standard techniques. Within preferred embodiments, the T cells are derived from a patient, a related donor or an unrelated donor, and are administered to the patient following stimulation and expansion.

[0566] For therapeutic purposes, CD4⁺ or CD8⁺ T cells that proliferate in response to a tumor polypeptide, polynucleotide or APC can be expanded in number either in vitro or in vivo. Proliferation of such T cells in vitro may be accomplished in a variety of ways. For example, the T cells can be re-exposed to a tumor polypeptide, or a short peptide corresponding to an immunogenic portion of such a polypeptide, with or without the addition of T cell growth factors, such as interleukin-2, and/or stimulator cells that synthesize a tumor polypeptide. Alternatively, one or more T cells that proliferate in the presence of the tumor polypeptide can be expanded in number by cloning. Methods for cloning cells are well known in the art, and include limiting dilution.

[0567] Pharmaceutical Compositions

[0568] In additional embodiments, the present invention concerns formulation of one or more of the polynucleotide, polypeptide, T-cell and/or antibody compositions disclosed herein in pharmaceutically-acceptable carriers for administration to a cell or an animal, either alone, or in combination with one or more other modalities of therapy.

[0569] It will be understood that, if desired, a composition as disclosed herein may be administered in combination with other agents as well, such as, e.g., other proteins or polypeptides or various pharmaceutically-active agents. In fact, there is virtually no limit to other components that may also be included, given that the additional agents do not cause a significant adverse effect upon contact with the target cells or host tissues. The compositions may thus be delivered along with various other agents as required in the particular instance. Such compositions may be purified from host cells or other biological sources, or alternatively may be chemically synthesized as described herein. Likewise, such compositions may further comprise substituted or derivatized RNA or DNA compositions.

[0570] Therefore, in another aspect of the present invention, pharmaceutical compositions are provided comprising one or more of the polynucleotide, polypeptide, antibody, and/or T-cell compositions described herein in combination with a physiologically acceptable carrier. In certain preferred embodiments, the pharmaceutical compositions of the invention comprise immunogenic polynucleotide and/or polypeptide compositions of the invention for use in prophylactic and theraputic vaccine applications. Vaccine preparation is generally described in, for example, M. F. Powell and M. J. Newman, eds., “Vaccine Design (the subunit and adjuvant approach),” Plenum Press (NY, 1995). Generally, such compositions will comprise one or more polynucleotide and/or polypeptide compositions of the present invention in combination with one or more immunostimulants.

[0571] It will be apparent that any of the pharmaceutical compositions described herein can contain pharmaceutically acceptable salts of the polynucleotides and polypeptides of the invention. Such salts can be prepared, for example, from pharmaceutically acceptable non-toxic bases, including organic bases (e.g., salts of primary, secondary and tertiary amines and basic amino acids) and inorganic bases (e.g., sodium, potassium, lithium, ammonium, calcium and magnesium salts).

[0572] In another embodiment, illustrative immunogenic compositions, e.g., vaccine compositions, of the present invention comprise DNA encoding one or more of the polypeptides as described above, such that the polypeptide is generated in situ. As noted above, the polynucleotide may be administered within any of a variety of delivery systems known to those of ordinary skill in the art. Indeed, numerous gene delivery techniques are well known in the art, such as those described by Rolland, Crit. Rev. Therap. Drug Carrier Systems 15:143-198, 1998, and references cited therein. Appropriate polynucleotide expression systems will, of course, contain the necessary regulatory DNA regulatory sequences for expression in a patient (such as a suitable promoter and terminating signal). Alternatively, bacterial delivery systems may involve the administration of a bacterium (such as Bacillus-Calmette-Guerrin) that expresses an immunogenic portion of the polypeptide on its cell surface or secretes such an epitope.

[0573] Therefore, in certain embodiments, polynucleotides encoding immunogenic polypeptides described herein are introduced into suitable mammalian host cells for expression using any of a number of known viral-based systems. In one illustrative embodiment, retroviruses provide a convenient and effective platform for gene delivery systems. A selected nucleotide sequence encoding a polypeptide of the present invention can be inserted into a vector and packaged in retroviral particles using techniques known in the art. The recombinant virus can then be isolated and delivered to a subject. A number of illustrative retroviral systems have been described (e.g., U.S. Pat. No. 5,219,740; Miller and Rosman (1989) BioTechniques 7:980-990; Miller, A. D. (1990) Human Gene Therapy 1:5-14; Scarpa et al. (1991) Virology 180:849-852; Burns et al. (1993) Proc. Natl. Acad. Sci. USA 90:8033-8037; and Boris-Lawrie and Temin (1993) Cur. Opin. Genet. Develop. 3:102-109.

[0574] In addition, a number of illustrative adenovirus-based systems have also been described. Unlike retroviruses which integrate into the host genome, adenoviruses persist extrachromosomally thus minimizing the risks associated with insertional mutagenesis (Haj-Ahmad and Graham (1986) J. Virol. 57:267-274; Bett et al. (1993) J. Virol. 67:5911-5921; Mittereder et al. (1994) Human Gene Therapy 5:717-729; Seth et al. (1994) J. Virol. 68:933-940; Barr et al. (1994) Gene Therapy 1:51-58; Berkner, K. L. (1988) BioTechniques 6:616-629; and Rich et al. (1993) Human Gene Therapy 4:461-476).

[0575] Various adeno-associated virus (AAV) vector systems have also been developed for polynucleotide delivery. AAV vectors can be readily constructed using techniques well known in the art. See, e.g., U.S. Pat. Nos. 5,173,414 and 5,139,941; International Publication Nos. WO 92/01070 and WO 93/03769; Lebkowski et al. (1988) Molec. Cell. Biol. 8:3988-3996; Vincent et al. (1990) Vaccines 90 (Cold Spring Harbor Laboratory Press); Carter, B. J. (1992) Current Opinion in Biotechnology 3:533-539; Muzyczka, N. (1992) Current Topics in Microbiol. and Immunol. 158:97-129; Kotin, R. M. (1994) Human Gene Therapy 5:793-801; Shelling and Smith (1994) Gene Therapy 1:165-169; and Zhou et al. (1994) J. Exp. Med. 179:1867-1875.

[0576] Additional viral vectors useful for delivering the polynucleotides encoding polypeptides of the present invention by gene transfer include those derived from the pox family of viruses, such as vaccinia virus and avian poxvirus. By way of example, vaccinia virus recombinants expressing the novel molecules can be constructed as follows. The DNA encoding a polypeptide is first inserted into an appropriate vector so that it is adjacent to a vaccinia promoter and flanking vaccinia DNA sequences, such as the sequence encoding thymidine kinase (TK). This vector is then used to transfect cells which are simultaneously infected with vaccinia. Homologous recombination serves to insert the vaccinia promoter plus the gene encoding the polypeptide of interest into the viral genome. The resulting TK.sup.(−) recombinant can be selected by culturing the cells in the presence of 5-bromodeoxyuridine and picking viral plaques resistant thereto.

[0577] A vaccinia-based infection/transfection system can be conveniently used to provide for inducible, transient expression or coexpression of one or more polypeptides described herein in host cells of an organism. In this particular system, cells are first infected in vitro with a vaccinia virus recombinant that encodes the bacteriophage T7 RNA polymerase. This polymerase displays exquisite specificity in that it only transcribes templates bearing T7 promoters. Following infection, cells are transfected with the polynucleotide or polynucleotides of interest, driven by a T7 promoter. The polymerase expressed in the cytoplasm from the vaccinia virus recombinant transcribes the transfected DNA into RNA which is then translated into polypeptide by the host translational machinery. The method provides for high level, transient, cytoplasmic production of large quantities of RNA and its translation products. See, e.g., Elroy-Stein and Moss, Proc. Natl. Acad. Sci. USA (1990) 87:6743-6747; Fuerst et al. Proc. Natl. Acad. Sci. USA (1986) 83:8122-8126.

[0578] Alternatively, avipoxviruses, such as the fowlpox and canarypox viruses, can also be used to deliver the coding sequences of interest. Recombinant avipox viruses, expressing immunogens from mammalian pathogens, are known to confer protective immunity when administered to non-avian species. The use of an Avipox vector is particularly desirable in human and other mammalian species since members of the Avipox genus can only productively replicate in susceptible avian species and therefore are not infective in mammalian cells. Methods for producing recombinant Avipoxviruses are known in the art and employ genetic recombination, as described above with respect to the production of vaccinia viruses. See, e.g., WO 91/12882; WO 89/03429; and WO 92/03545.

[0579] Any of a number of alphavirus vectors can also be used for delivery of polynucleotide compositions of the present invention, such as those vectors described in U.S. Pat. Nos. 5,843,723; 6,015,686; 6,008,035 and 6,015,694. Certain vectors based on Venezuelan Equine Encephalitis (VEE) can also be used, illustrative examples of which can be found in U.S. Pat. Nos. 5,505,947 and 5,643,576.

[0580] Moreover, molecular conjugate vectors, such as the adenovirus chimeric vectors described in Michael et al. J. Biol. Chem. (1993) 268:6866-6869 and Wagner et al. Proc. Natl. Acad. Sci. USA (1992) 89:6099-6103, can also be used for gene delivery under the invention.

[0581] Additional illustrative information on these and other known viral-based delivery systems can be found, for example, in Fisher-Hoch et al., Proc. Natl. Acad. Sci. USA 86:317-321, 1989; Flexner et al., Ann. N.Y Acad. Sci. 569:86-103, 1989; Flexner et al., Vaccine 8:17-21, 1990; U.S. Pat. Nos. 4,603,112, 4,769,330, and 5,017,487; WO 89/01973; U.S. Pat. No. 4,777,127; GB 2,200,651; EP 0,345,242; WO 91/02805; Berkner, Biotechniques 6:616-627, 1988; Rosenfeld et al., Science 252:431-434, 1991; Kolls et al., Proc. Natl. Acad. Sci. USA 91:215-219, 1994; Kass-Eisler et al., Proc. Natl. Acad. Sci. USA 90:11498-11502, 1993; Guzman et al., Circulation 88:2838-2848, 1993; and Guzman et al., Cir. Res. 73:1202-1207, 1993.

[0582] In certain embodiments, a polynucleotide may be integrated into the genome of a target cell. This integration may be in the specific location and orientation via homologous recombination (gene replacement) or it may be integrated in a random, non-specific location (gene augmentation). In yet further embodiments, the polynucleotide may be stably maintained in the cell as a separate, episomal segment of DNA. Such polynucleotide segments or “episomes” encode sequences sufficient to permit maintenance and replication independent of or in synchronization with the host cell cycle. The manner in which the expression construct is delivered to a cell and where in the cell the polynucleotide remains is dependent on the type of expression construct employed.

[0583] In another embodiment of the invention, a polynucleotide is administered/delivered as “naked” DNA, for example as described in Ulmer et al., Science 259:1745-1749, 1993 and reviewed by Cohen, Science 259:1691-1692, 1993. The uptake of naked DNA may be increased by coating the DNA onto biodegradable beads, which are efficiently transported into the cells.

[0584] In still another embodiment, a composition of the present invention can be delivered via a particle bombardment approach, many of which have been described. In one illustrative example, gas-driven particle acceleration can be achieved with devices such as those manufactured by Powderject Pharmaceuticals PLC (Oxford, UK) and Powderject Vaccines Inc. (Madison, Wis.), some examples of which are described in U.S. Pat. Nos. 5,846,796; 6,010,478; 5,865,796; 5,584,807; and EP Pat. No. 0500 799. This approach offers a needle-free delivery approach wherein a dry powder formulation of microscopic particles, such as polynucleotide or polypeptide particles, are accelerated to high speed within a helium gas jet generated by a hand held device, propelling the particles into a target tissue of interest.

[0585] In a related embodiment, other devices and methods that may be useful for gas-driven needle-less injection of compositions of the present invention include those provided by Bioject, Inc. (Portland, Oreg.), some examples of which are described in U.S. Pat. Nos. 4,790,824; 5,064,413; 5,312,335; 5,383,851; 5,399,163; 5,520,639 and 5,993,412.

[0586] According to another embodiment, the pharmaceutical compositions described herein will comprise one or more immunostimulants in addition to the immunogenic polynucleotide, polypeptide, antibody, T-cell and/or APC compositions of this invention. An immunostimulant refers to essentially any substance that enhances or potentiates an immune response (antibody and/or cell-mediated) to an exogenous antigen. One preferred type of immunostimulant comprises an adjuvant. Many adjuvants contain a substance designed to protect the antigen from rapid catabolism, such as aluminum hydroxide or mineral oil, and a stimulator of immune responses, such as lipid A, Bortadella pertussis or Mycobacterium tuberculosis derived proteins. Certain adjuvants are commercially available as, for example, Freund's Incomplete Adjuvant and Complete Adjuvant (Difco Laboratories, Detroit, Mich.); Merck Adjuvant 65 (Merck and Company, Inc., Rahway, N.J.); AS-2 (SmithKline Beecham, Philadelphia, Pa.); aluminum salts such as aluminum hydroxide gel (alum) or aluminum phosphate; salts of calcium, iron or zinc; an insoluble suspension of acylated tyrosine; acylated sugars; cationically or anionically derivatized polysaccharides; polyphosphazenes; biodegradable microspheres; monophosphoryl lipid A and quil A. Cytokines, such as GM-CSF, interleukin-2, -7, -12, and other like growth factors, may also be used as adjuvants.

[0587] Within certain embodiments of the invention, the adjuvant composition is preferably one that induces an immune response predominantly of the Th1 type. High levels of Th1-type cytokines (e.g., IFN-γ, TNFα, IL-2 and IL-12) tend to favor the induction of cell mediated immune responses to an administered antigen. In contrast, high levels of Th2-type cytokines (e.g., IL-4, IL-5, IL-6 and IL-10) tend to favor the induction of humoral immune responses. Following application of a vaccine as provided herein, a patient will support an immune response that includes Th1- and Th2-type responses. Within a preferred embodiment, in which a response is predominantly Th1-type, the level of Th1-type cytokines will increase to a greater extent than the level of Th2-type cytokines. The levels of these cytokines may be readily assessed using standard assays. For a review of the families of cytokines, see Mosmann and Coffinan, Ann. Rev. Immunol. 7:145-173, 1989.

[0588] Certain preferred adjuvants for eliciting a predominantly Th1-type response include, for example, a combination of monophosphoryl lipid A, preferably 3-de-O-acylated monophosphoryl lipid A, together with an aluminum salt. MPL® adjuvants are available from Corixa Corporation (Seattle, Wash.; see, for example, U.S. Pat. Nos. 4,436,727; 4,877,611; 4,866,034 and 4,912,094). CpG-containing oligonucleotides (in which the CpG dinucleotide is unmethylated) also induce a predominantly Th1 response. Such oligonucleotides are well known and are described, for example, in WO 96/02555, WO 99/33488 and U.S. Pat. Nos. 6,008,200 and 5,856,462. Immunostimulatory DNA sequences are also described, for example, by Sato et al., Science 273:352, 1996. Another preferred adjuvant comprises a saponin, such as Quil A, or derivatives thereof, including QS21 and QS7 (Aquila Biopharmaceuticals Inc., Framingham, Mass.); Escin; Digitonin; or Gypsophila or Chenopodium quinoa saponins. Other preferred formulations include more than one saponin in the adjuvant combinations of the present invention, for example combinations of at least two of the following group comprising QS21, QS7, Quil A, β-escin, or digitonin.

[0589] Alternatively the saponin formulations may be combined with vaccine vehicles composed of chitosan or other polycationic polymers, polylactide and polylactide-co-glycolide particles, poly-N-acetyl glucosamine-based polymer matrix, particles composed of polysaccharides or chemically modified polysaccharides, liposomes and lipid-based particles, particles composed of glycerol monoesters, etc. The saponins may also be formulated in the presence of cholesterol to form particulate structures such as liposomes or ISCOMs. Furthermore, the saponins may be formulated together with a polyoxyethylene ether or ester, in either a non-particulate solution or suspension, or in a particulate structure such as a paucilamelar liposome or ISCOM. The saponins may also be formulated with excipients such as Carbopol^(R) to increase viscosity, or may be formulated in a dry powder form with a powder excipient such as lactose.

[0590] In one preferred embodiment, the adjuvant system includes the combination of a monophosphoryl lipid A and a saponin derivative, such as the combination of QS21 and 3D-MPL® adjuvant, as described in WO 94/00153, or a less reactogenic composition where the QS21 is quenched with cholesterol, as described in WO 96/33739. Other preferred formulations comprise an oil-in-water emulsion and tocopherol. Another particularly preferred adjuvant formulation employing QS21, 3D-MPL® adjuvant and tocopherol in an oil-in-water emulsion is described in WO 95/17210.

[0591] Another enhanced adjuvant system involves the combination of a CpG-containing oligonucleotide and a saponin derivative particularly the combination of CpG and QS21 is disclosed in WO 00/09159. Preferably the formulation additionally comprises an oil in water emulsion and tocopherol.

[0592] Additional illustrative adjuvants for use in the pharmaceutical compositions of the invention include Montanide ISA 720 (Seppic, France), SAF (Chiron, Calif., United States), ISCOMS (CSL), MF-59 (Chiron), the SBAS series of adjuvants (e.g., SBAS-2 or SBAS-4, available from SmithKline Beecham, Rixensart, Belgium), Detox (Enhanzyn®) (Corixa, Hamilton, Mont.T), RC-529 (Corixa, Hamilton, Mont.) and other arninoalkyl glucosaminide 4-phosphates (AGPs), such as those described in pending U.S. patent application Ser. Nos. 08/853,826 and 09/074,720, the disclosures of which are incorporated herein by reference in their entireties, and polyoxyethylene ether adjuvants such as those described in WO 99/52549A1.

[0593] Other preferred adjuvants include adjuvant molecules of the general formula

[0594] (I): HO(CH₂CH₂O)_(n)—A—R,

[0595] wherein, n is 1-50, A is a bond or —C(O)—, R is C₁₋₅₀ alkyl or Phenyl C₁₋₅₀ alkyl.

[0596] One embodiment of the present invention consists of a vaccine formulation comprising a polyoxyethylene ether of general formula (I), wherein n is between 1 and 50, preferably 4-24, most preferably 9; the R component is C₁₋₅₀, preferably C₄-C₂₀ alkyl and most preferably C₁₂ alkyl, and A is a bond. The concentration of the polyoxyethylene ethers should be in the range 0.1-20%, preferably from 0.1-10%, and most preferably in the range 0.1-1%. Preferred polyoxyethylene ethers are selected from the following group: polyoxyethylene-9-lauryl ether, polyoxyethylene-9-steoryl ether, polyoxyethylene-8-steoryl ether, polyoxyethylene-4-lauryl ether, polyoxyethylene-35-lauryl ether, and polyoxyethylene-23-lauryl ether. Polyoxyethylene ethers such as polyoxyethylene lauryl ether are described in the Merck index (12^(th) edition: entry 7717). These adjuvant molecules are described in WO 99/52549.

[0597] The polyoxyethylene ether according to the general formula (I) above may, if desired, be combined with another adjuvant. For example, a preferred adjuvant combination is preferably with CpG as described in the pending UK patent application GB 9820956.2.

[0598] According to another embodiment of this invention, an immunogenic composition described herein is delivered to a host via antigen presenting cells (APCs), such as dendritic cells, macrophages, B cells, monocytes and other cells that may be engineered to be efficient APCs. Such cells may, but need not, be genetically modified to increase the capacity for presenting the antigen, to improve activation and/or maintenance of the T cell response, to have anti-tumor effects per se and/or to be immunologically compatible with the receiver (ie., matched HLA haplotype). APCs may generally be isolated from any of a variety of biological fluids and organs, including tumor and peritumoral tissues, and may be autologous, allogeneic, syngeneic or xenogeneic cells.

[0599] Certain preferred embodiments of the present invention use dendritic cells or progenitors thereof as antigen-presenting cells. Dendritic cells are highly potent APCs (Banchereau and Steinman, Nature 392:245-251, 1998) and have been shown to be effective as a physiological adjuvant for eliciting prophylactic or therapeutic antitumor immunity (see Timmerman and Levy, Ann. Rev. Med. 50:507-529, 1999). In general, dendritic cells may be identified based on their typical shape (stellate in situ, with marked cytoplasmic processes (dendrites) visible in vitro), their ability to take up, process and present antigens with high efficiency and their ability to activate naïve T cell responses. Dendritic cells may, of course, be engineered to express specific cell-surface receptors or ligands that are not commonly found on dendritic cells in vivo or ex vivo, and such modified dendritic cells are contemplated by the present invention. As an alternative to dendritic cells, secreted vesicles antigen-loaded dendritic cells (called exosomes) may be used within a vaccine (see Zitvogel et al., Nature Med. 4:594-600, 1998).

[0600] Dendritic cells and progenitors may be obtained from peripheral blood, bone marrow, tumor-infiltrating cells, peritumoral tissues-infiltrating cells, lymph nodes, spleen, skin, umbilical cord blood or any other suitable tissue or fluid. For example, dendritic cells may be differentiated ex vivo by adding a combination of cytokines such as GM-CSF, IL-4, IL-13 and/or TNFα to cultures of monocytes harvested from peripheral blood. Alternatively, CD34 positive cells harvested from peripheral blood, umbilical cord blood or bone marrow may be differentiated into dendritic cells by adding to the culture medium combinations of GM-CSF, IL-3, TNFα, CD40 ligand, LPS, flt3 ligand and/or other compound(s) that induce differentiation, maturation and proliferation of dendritic cells.

[0601] Dendritic cells are conveniently categorized as “immature” and “mature” cells, which allows a simple way to discriminate between two well characterized phenotypes. However, this nomenclature should not be construed to exclude all possible intermediate stages of differentiation. Immature dendritic cells are characterized as APC with a high capacity for antigen uptake and processing, which correlates with the high expression of Fcγ receptor and mannose receptor. The mature phenotype is typically characterized by a lower expression of these markers, but a high expression of cell surface molecules responsible for T cell activation such as class I and class II MHC, adhesion molecules (e.g., CD54 and CD11) and costimulatory molecules (e.g., CD40, CD80, CD86 and 4-1BB).

[0602] APCs may generally be transfected with a polynucleotide of the invention (or portion or other variant thereof) such that the encoded polypeptide, or an immunogenic portion thereof, is expressed on the cell surface. Such transfection may take place ex vivo, and a pharmaceutical composition comprising such transfected cells may then be used for therapeutic purposes, as described herein. Alternatively, a gene delivery vehicle that targets a dendritic or other antigen presenting cell may be administered to a patient, resulting in transfection that occurs in vivo. In vivo and ex vivo transfection of dendritic cells, for example, may generally be performed using any methods known in the art, such as those described in WO 97/24447, or the gene gun approach described by Mahvi et al., Immunology and cell Biology 75:456-460, 1997. Antigen loading of dendritic cells may be achieved by incubating dendritic cells or progenitor cells with the tumor polypeptide, DNA (naked or within a plasmid vector) or RNA; or with antigen-expressing recombinant bacterium or viruses (e.g., vaccinia, fowlpox, adenovirus or lentivirus vectors). Prior to loading, the polypeptide may be covalently conjugated to an immunological partner that provides T cell help (e.g., a carrier molecule). Alternatively, a dendritic cell may be pulsed with a non-conjugated immunological partner, separately or in the presence of the polypeptide.

[0603] While any suitable carrier known to those of ordinary skill in the art may be employed in the pharmaceutical compositions of this invention, the type of carrier will typically vary depending on the mode of administration. Compositions of the present invention may be formulated for any appropriate manner of administration, including for example, topical, oral, nasal, mucosal, intravenous, intracranial, intraperitoneal, subcutaneous and intramuscular administration.

[0604] Carriers for use within such pharmaceutical compositions are biocompatible, and may also be biodegradable. In certain embodiments, the formulation preferably provides a relatively constant level of active component release. In other embodiments, however, a more rapid rate of release immediately upon administration may be desired. The formulation of such compositions is well within the level of ordinary skill in the art using known techniques. Illustrative carriers useful in this regard include microparticles of poly(lactide-co-glycolide), polyacrylate, latex, starch, cellulose, dextran and the like. Other illustrative delayed-release carriers include supramolecular biovectors, which comprise a non-liquid hydrophilic core (e.g., a cross-linked polysaccharide or oligosaccharide) and, optionally, an external layer comprising an amphiphilic compound, such as a phospholipid (see e.g., U.S. Pat. No. 5,151,254 and PCT applications WO 94/20078, WO/94/23701 and WO 96/06638). The amount of active compound contained within a sustained release formulation depends upon the site of implantation, the rate and expected duration of release and the nature of the condition to be treated or prevented.

[0605] In another illustrative embodiment, biodegradable microspheres (e.g., polylactate polyglycolate) are employed as carriers for the compositions of this invention. Suitable biodegradable microspheres are disclosed, for example, in U.S. Pat. Nos. 4,897,268; 5,075,109; 5,928,647; 5,811,128; 5,820,883; 5,853,763; 5,814,344, 5,407,609 and 5,942,252. Modified hepatitis B core protein carrier systems, such as described in WO/99 40934, and references cited therein, will also be useful for many applications. Another illustrative carrier/delivery system employs a carrier comprising particulate-protein complexes, such as those described in U.S. Pat. No. 5,928,647, which are capable of inducing a class I-restricted cytotoxic T lymphocyte responses in a host.

[0606] The pharmaceutical compositions of the invention will often further comprise one or more buffers (e.g., neutral buffered saline or phosphate buffered saline), carbohydrates (e.g., glucose, mannose, sucrose or dextrans), mannitol, proteins, polypeptides or amino acids such as glycine, antioxidants, bacteriostats, chelating agents such as EDTA or glutathione, adjuvants (e.g., aluminum hydroxide), solutes that render the formulation isotonic, hypotonic or weakly hypertonic with the blood of a recipient, suspending agents, thickening agents and/or preservatives. Alternatively, compositions of the present invention may be formulated as a lyophilizate.

[0607] The pharmaceutical compositions described herein may be presented in unit-dose or multi-dose containers, such as sealed ampoules or vials. Such containers are typically sealed in such a way to preserve the sterility and stability of the formulation until use. In general, formulations may be stored as suspensions, solutions or emulsions in oily or aqueous vehicles. Alternatively, a pharmaceutical composition may be stored in a freeze-dried condition requiring only the addition of a sterile liquid carrier immediately prior to use.

[0608] The development of suitable dosing and treatment regimens for using the particular compositions described herein in a variety of treatment regimens, including e.g., oral, parenteral, intravenous, intranasal, and intramuscular administration and formulation, is well known in the art, some of which are briefly discussed below for general purposes of illustration.

[0609] In certain applications, the pharmaceutical compositions disclosed herein may be delivered via oral administration to an animal. As such, these compositions may be formulated with an inert diluent or with an assimilable edible carrier, or they may be enclosed in hard- or soft-shell gelatin capsule, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet.

[0610] The active compounds may even be incorporated with excipients and used in the form of ingestible tablets, buccal tables, troches, capsules, elixirs, suspensions, syrups, wafers, and the like (see, for example, Mathiowitz et al., Nature 1997 March 27;386(6623):410-4; Hwang et al., Crit Rev Ther Drug Carrier Syst 1998;15(3):243-84; U.S. Pat. No. 5,641,515; U.S. Pat. No. 5,580,579 and U.S. Pat. No. 5,792,451). Tablets, troches, pills, capsules and the like may also contain any of a variety of additional components, for example, a binder, such as gum tragacanth, acacia, cornstarch, or gelatin; excipients, such as dicalcium phosphate; a disintegrating agent, such as corn starch, potato starch, alginic acid and the like; a lubricant, such as magnesium stearate; and a sweetening agent, such as sucrose, lactose or saccharin may be added or a flavoring agent, such as peppermint, oil of wintergreen, or cherry flavoring. When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar, or both. Of course, any material used in preparing any dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed. In addition, the active compounds may be incorporated into sustained-release preparation and formulations.

[0611] Typically, these formulations will contain at least about 0.1% of the active compound or more, although the percentage of the active ingredient(s) may, of course, be varied and may conveniently be between about 1 or 2% and about 60% or 70% or more of the weight or volume of the total formulation. Naturally, the amount of active compound(s) in each therapeutically useful composition may be prepared is such a way that a suitable dosage will be obtained in any given unit dose of the compound. Factors such as solubility, bioavailability, biological half-life, route of administration, product shelf life, as well as other pharmacological considerations will be contemplated by one skilled in the art of preparing such pharmaceutical formulations, and as such, a variety of dosages and treatment regimens may be desirable.

[0612] For oral administration the compositions of the present invention may alternatively be incorporated with one or more excipients in the form of a mouthwash, dentifrice, buccal tablet, oral spray, or sublingual orally-administered formulation. Alternatively, the active ingredient may be incorporated into an oral solution such as one containing sodium borate, glycerin and potassium bicarbonate, or dispersed in a dentifrice, or added in a therapeutically-effective amount to a composition that may include water, binders, abrasives, flavoring agents, foaming agents, and humectants. Alternatively the compositions may be fashioned into a tablet or solution form that may be placed under the tongue or otherwise dissolved in the mouth.

[0613] In certain circumstances it will be desirable to deliver the pharmaceutical compositions disclosed herein parenterally, intravenously, intramuscularly, or even intraperitoneally. Such approaches are well known to the skilled artisan, some of which are further described, for example, in U.S. Pat. No. 5,543,158; U.S. Pat. No. 5,641,515 and U.S. Pat. No. 5,399,363. In certain embodiments, solutions of the active compounds as free base or pharmacologically acceptable salts may be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose. Dispersions may also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations generally will contain a preservative to prevent the growth of microorganisms.

[0614] Illustrative pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions (for example, see U.S. Pat. No. 5,466,468). In all cases the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and/or vegetable oils. Proper fluidity may be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and/or by the use of surfactants. The prevention of the action of microorganisms can be facilitated by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

[0615] In one embodiment, for parenteral administration in an aqueous solution, the solution should be suitably buffered if necessary and the liquid diluent first rendered isotonic with sufficient saline or glucose. These particular aqueous solutions are especially suitable for intravenous, intramuscular, subcutaneous and intraperitoneal administration. In this connection, a sterile aqueous medium that can be employed will be known to those of skill in the art in light of the present disclosure. For example, one dosage may be dissolved in 1 ml of isotonic NaCl solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion, (see for example, “Remington's Pharmaceutical Sciences” 15th Edition, pages 1035-1038 and 1570-1580). Some variation in dosage will necessarily occur depending on the condition of the subject being treated. Moreover, for human administration, preparations will of course preferably meet sterility, pyrogenicity, and the general safety and purity standards as required by FDA Office of Biologics standards.

[0616] In another embodiment of the invention, the compositions disclosed herein may be formulated in a neutral or salt form. Illustrative pharmaceutically-acceptable salts include the acid addition salts (formed with the free amino groups of the protein) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, histidine, procaine and the like. Upon formulation, solutions will be administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective.

[0617] The carriers can further comprise any and all solvents, dispersion media, vehicles, coatings, diluents, antibacterial and antifungal agents, isotonic and absorption delaying agents, buffers, carrier solutions, suspensions, colloids, and the like. The use of such media and agents for pharmaceutical active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions. The phrase “pharmaceutically-acceptable” refers to molecular entities and compositions that do not produce an allergic or similar untoward reaction when administered to a human.

[0618] In certain embodiments, the pharmaceutical compositions may be delivered by intranasal sprays, inhalation, and/or other aerosol delivery vehicles. Methods for delivering genes, nucleic acids, and peptide compositions directly to the lungs via nasal aerosol sprays has been described, e.g., in U.S. Pat. No. 5,756,353 and U.S. Pat. No. 5,804,212. Likewise, the delivery of drugs using intranasal microparticle resins (Takenaga et al., J Controlled Release 1998 March 2;52(1-2):81-7) and lysophosphatidyl-glycerol compounds (U.S. Pat. No. 5,725,871) are also well-known in the pharmaceutical arts. Likewise, illustrative transmucosal drug delivery in the form of a polytetrafluoroetheylene support matrix is described in U.S. Pat. No. 5,780,045.

[0619] In certain embodiments, liposomes, nanocapsules, microparticles, lipid particles, vesicles, and the like, are used for the introduction of the compositions of the present invention into suitable host cells/organisms. In particular, the compositions of the present invention may be formulated for delivery either encapsulated in a lipid particle, a liposome, a vesicle, a nanosphere, or a nanoparticle or the like. Alternatively, compositions of the present invention can be bound, either covalently or non-covalently, to the surface of such carrier vehicles.

[0620] The formation and use of liposome and liposome-like preparations as potential drug carriers is generally known to those of skill in the art (see for example, Lasic, Trends Biotechnol 1998 July; 16(7):307-21; Takakura, Nippon Rinsho 1998 March;56(3):691-5; Chandran et al., Indian J Exp Biol. 1997 August;35(8):801-9; Margalit, Crit Rev Ther Drug Carrier Syst. 1995;12(2-3):233-61; U.S. Pat. No. 5,567,434; U.S. Pat. No. 5,552,157; U.S. Pat. No. 5,565,213; U.S. Pat. No. 5,738,868 and U.S. Pat. No. 5,795,587, each specifically incorporated herein by reference in its entirety).

[0621] Liposomes have been used successfully with a number of cell types that are normally difficult to transfect by other procedures, including T cell suspensions, primary hepatocyte cultures and PC 12 cells (Renneisen et al., J Biol Chem. 1990 September 25;265(27):16337-42; Muller et al., DNA Cell Biol. 1990 April;9(3):221-9). In addition, liposomes are free of the DNA length constraints that are typical of viral-based delivery systems. Liposomes have been used effectively to introduce genes, various drugs, radiotherapeutic agents, enzymes, viruses, transcription factors, allosteric effectors and the like, into a variety of cultured cell lines and animals. Furthermore, he use of liposomes does not appear to be associated with autoimmune responses or unacceptable toxicity after systemic delivery.

[0622] In certain embodiments, liposomes are formed from phospholipids that are dispersed in an aqueous medium and spontaneously form multilamellar concentric bilayer vesicles (also termed multilamellar vesicles (MLVs).

[0623] Alternatively, in other embodiments, the invention provides for pharmaceutically-acceptable nanocapsule formulations of the compositions of the present invention. Nanocapsules can generally entrap compounds in a stable and reproducible way (see, for example, Quintanar-Guerrero et al., Drug Dev Ind Pharm. 1998 December;24(12):1113-28). To avoid side effects due to intracellular polymeric overloading, such ultrafine particles (sized around 0.1 μm) may be designed using polymers able to be degraded in vivo. Such particles can be made as described, for example, by Couvreur et al., Crit Rev Ther Drug Carrier Syst. 1988;5(1):1-20; zur Muhlen et al., Eur J Pharm Biopharm. 1998 March;45(2):149-55; Zambaux et al. J Controlled Release. 1998 January 2;50(1-3):31-40; and U.S. Pat. No. 5,145,684.

[0624] Cancer Therapeutic Methods

[0625] In further aspects of the present invention, the pharmaceutical compositions described herein may be used for the treatment of cancer, particularly for the immunotherapy of lung cancer. Within such methods, the pharmaceutical compositions described herein are administered to a patient, typically a warm-blooded animal, preferably a human. A patient may or may not be afflicted with cancer. Accordingly, the above pharmaceutical compositions may be used to prevent the development of a cancer or to treat a patient afflicted with a cancer. Pharmaceutical compositions and vaccines may be administered either prior to or following surgical removal of primary tumors and/or treatment such as administration of radiotherapy or conventional chemotherapeutic drugs. As discussed above, administration of the pharmaceutical compositions may be by any suitable method, including administration by intravenous, intraperitoneal, intramuscular, subcutaneous, intranasal, intradermal, anal, vaginal, topical and oral routes.

[0626] Within certain embodiments, immunotherapy may be active immunotherapy, in which treatment relies on the in vivo stimulation of the endogenous host immune system to react against tumors with the administration of immune response-modifying agents (such as polypeptides and polynucleotides as provided herein).

[0627] Within other embodiments, immunotherapy may be passive immunotherapy, in which treatment involves the delivery of agents with established tumor-immune reactivity (such as effector cells or antibodies) that can directly or indirectly mediate antitumor effects and does not necessarily depend on an intact host immune system. Examples of effector cells include T cells as discussed above, T lymphocytes (such as CD8⁺ cytotoxic T lymphocytes and CD4⁺ T-helper tumor-infiltrating lymphocytes), killer cells (such as Natural Killer cells and lymphokine-activated killer cells), B cells and antigen-presenting cells (such as dendritic cells and macrophages) expressing a polypeptide provided herein. T cell receptors and antibody receptors specific for the polypeptides recited herein may be cloned, expressed and transferred into other vectors or effector cells for adoptive immunotherapy. The polypeptides provided herein may also be used to generate antibodies or anti-idiotypic antibodies (as described above and in U.S. Pat. No. 4,918,164) for passive immunotherapy.

[0628] Effector cells may generally be obtained in sufficient quantities for adoptive immunotherapy by growth in vitro, as described herein. Culture conditions for expanding single antigen-specific effector cells to several billion in number with retention of antigen recognition in vivo are well known in the art. Such in vitro culture conditions typically use intermittent stimulation with antigen, often in the presence of cytokines (such as IL-2) and non-dividing feeder cells. As noted above, immunoreactive polypeptides as provided herein may be used to rapidly expand antigen-specific T cell cultures in order to generate a sufficient number of cells for immunotherapy. In particular, antigen-presenting cells, such as dendritic, macrophage, monocyte, fibroblast and/or B cells, may be pulsed with immunoreactive polypeptides or transfected with one or more polynucleotides using standard techniques well known in the art. For example, antigen-presenting cells can be transfected with a polynucleotide having a promoter appropriate for increasing expression in a recombinant virus or other expression system. Cultured effector cells for use in therapy must be able to grow and distribute widely, and to survive long term in vivo. Studies have shown that cultured effector cells can be induced to grow in vivo and to survive long term in substantial numbers by repeated stimulation with antigen supplemented with IL-2 (see, for example, Cheever et al., Immunological Reviews 157:177, 1997).

[0629] Alternatively, a vector expressing a polypeptide recited herein may be introduced into antigen presenting cells taken from a patient and clonally propagated ex vivo for transplant back into the same patient. Transfected cells may be reintroduced into the patient using any means known in the art, preferably in sterile form by intravenous, intracavitary, intraperitoneal or intratumor administration.

[0630] Routes and frequency of administration of the therapeutic compositions described herein, as well as dosage, will vary from individual to individual, and may be readily established using standard techniques. In general, the pharmaceutical compositions and vaccines may be administered by injection (e.g., intracutaneous, intramuscular, intravenous or subcutaneous), intranasally (e.g., by aspiration) or orally. Preferably, between 1 and 10 doses may be administered over a 52 week period. Preferably, 6 doses are administered, at intervals of 1 month, and booster vaccinations may be given periodically thereafter. Alternate protocols may be appropriate for individual patients. A suitable dose is an amount of a compound that, when administered as described above, is capable of promoting an anti-tumor immune response, and is at least 10-50% above the basal (i.e., untreated) level. Such response can be monitored by measuring the anti-tumor antibodies in a patient or by vaccine-dependent generation of cytolytic effector cells capable of killing the patient's tumor cells in vitro. Such vaccines should also be capable of causing an immune response that leads to an improved clinical outcome (e.g., more frequent remissions, complete or partial or longer disease-free survival) in vaccinated patients as compared to non-vaccinated patients. In general, for pharmaceutical compositions and vaccines comprising one or more polypeptides, the amount of each polypeptide present in a dose ranges from about 25 μg to 5 mg per kg of host. Suitable dose sizes will vary with the size of the patient, but will typically range from about 0.1 mL to about 5 mL.

[0631] In general, an appropriate dosage and treatment regimen provides the active compound(s) in an amount sufficient to provide therapeutic and/or prophylactic benefit. Such a response can be monitored by establishing an improved clinical outcome (e.g., more frequent remissions, complete or partial, or longer disease-free survival) in treated patients as compared to non-treated patients. Increases in preexisting immune responses to a tumor protein generally correlate with an improved clinical outcome. Such immune responses may generally be evaluated using standard proliferation, cytotoxicity or cytokine assays, which may be performed using samples obtained from a patient before and after treatment.

[0632] Cancer Detection and Diagnostic Compositions, Methods and Kits

[0633] In general, a cancer may be detected in a patient based on the presence of one or more lung tumor proteins and/or polynucleotides encoding such proteins in a biological sample (for example, blood, sera, sputum urine and/or tumor biopsies) obtained from the patient. In other words, such proteins may be used as markers to indicate the presence or absence of a cancer such as lung cancer. In addition, such proteins may be useful for the detection of other cancers. The binding agents provided herein generally permit detection of the level of antigen that binds to the agent in the biological sample. Polynucleotide primers and probes may be used to detect the level of mRNA encoding a tumor protein, which is also indicative of the presence or absence of a cancer. In general, a lung tumor sequence should be present at a level that is at least three fold higher in tumor tissue than in normal tissue

[0634] There are a variety of assay formats known to those of ordinary skill in the art for using a binding agent to detect polypeptide markers in a sample. See, e.g., Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988. In general, the presence or absence of a cancer in a patient may be determined by (a) contacting a biological sample obtained from a patient with a binding agent; (b) detecting in the sample a level of polypeptide that binds to the binding agent; and (c) comparing the level of polypeptide with a predetermined cut-off value.

[0635] In a preferred embodiment, the assay involves the use of binding agent immobilized on a solid support to bind to and remove the polypeptide from the remainder of the sample. The bound polypeptide may then be detected using a detection reagent that contains a reporter group and specifically binds to the binding agent/polypeptide complex. Such detection reagents may comprise, for example, a binding agent that specifically binds to the polypeptide or an antibody or other agent that specifically binds to the binding agent, such as an anti-immunoglobulin, protein G, protein A or a lectin. Alternatively, a competitive assay may be utilized, in which a polypeptide is labeled with a reporter group and allowed to bind to the immobilized binding agent after incubation of the binding agent with the sample. The extent to which components of the sample inhibit the binding of the labeled polypeptide to the binding agent is indicative of the reactivity of the sample with the immobilized binding agent. Suitable polypeptides for use within such assays include full length lung tumor proteins and polypeptide portions thereof to which the binding agent binds, as described above.

[0636] The solid support may be any material known to those of ordinary skill in the art to which the tumor protein may be attached. For example, the solid support may be a test well in a microtiter plate or a nitrocellulose or other suitable membrane. Alternatively, the support may be a bead or disc, such as glass, fiberglass, latex or a plastic material such as polystyrene or polyvinylchloride. The support may also be a magnetic particle or a fiber optic sensor, such as those disclosed, for example, in U.S. Pat. No. 5,359,681. The binding agent may be immobilized on the solid support using a variety of techniques known to those of skill in the art, which are amply described in the patent and scientific literature. In the context of the present invention, the term “immobilization” refers to both noncovalent association, such as adsorption, and covalent attachment (which may be a direct linkage between the agent and functional groups on the support or may be a linkage by way of a cross-linking agent). Immobilization by adsorption to a well in a microtiter plate or to a membrane is preferred. In such cases, adsorption may be achieved by contacting the binding agent, in a suitable buffer, with the solid support for a suitable amount of time. The contact time varies with temperature, but is typically between about 1 hour and about 1 day. In general, contacting a well of a plastic microtiter plate (such as polystyrene or polyvinylchloride) with an amount of binding agent ranging from about 10 ng to about 10 μg, and preferably about 100 ng to about 1 μg, is sufficient to immobilize an adequate amount of binding agent.

[0637] Covalent attachment of binding agent to a solid support may generally be achieved by first reacting the support with a bifunctional reagent that will react with both the support and a functional group, such as a hydroxyl or amino group, on the binding agent. For example, the binding agent may be covalently attached to supports having an appropriate polymer coating using benzoquinone or by condensation of an aldehyde group on the support with an amine and an active hydrogen on the binding partner (see, e.g., Pierce Immunotechnology Catalog and Handbook, 1991, at A12-A13).

[0638] In certain embodiments, the assay is a two-antibody sandwich assay. This assay may be performed by first contacting an antibody that has been immobilized on a solid support, commonly the well of a microtiter plate, with the sample, such that polypeptides within the sample are allowed to bind to the immobilized antibody. Unbound sample is then removed from the immobilized polypeptide-antibody complexes and a detection reagent (preferably a second antibody capable of binding to a different site on the polypeptide) containing a reporter group is added. The amount of detection reagent that remains bound to the solid support is then determined using a method appropriate for the specific reporter group.

[0639] More specifically, once the antibody is immobilized on the support as described above, the remaining protein binding sites on the support are typically blocked. Any suitable blocking agent known to those of ordinary skill in the art, such as bovine serum albumin or Tween 20™ (Sigma Chemical Co., St. Louis, Mo.). The immobilized antibody is then incubated with the sample, and polypeptide is allowed to bind to the antibody. The sample may be diluted with a suitable diluent, such as phosphate-buffered saline (PBS) prior to incubation. In general, an appropriate contact time (i.e., incubation time) is a period of time that is sufficient to detect the presence of polypeptide within a sample obtained from an individual with lung cancer. Preferably, the contact time is sufficient to achieve a level of binding that is at least about 95% of that achieved at equilibrium between bound and unbound polypeptide. Those of ordinary skill in the art will recognize that the time necessary to achieve equilibrium may be readily determined by assaying the level of binding that occurs over a period of time. At room temperature, an incubation time of about 30 minutes is generally sufficient.

[0640] Unbound sample may then be removed by washing the solid support with an appropriate buffer, such as PBS containing 0.1% Tween 20™. The second antibody, which contains a reporter group, may then be added to the solid support. Preferred reporter groups include those groups recited above.

[0641] The detection reagent is then incubated with the immobilized antibody-polypeptide complex for an amount of time sufficient to detect the bound polypeptide. An appropriate amount of time may generally be determined by assaying the level of binding that occurs over a period of time. Unbound detection reagent is then removed and bound detection reagent is detected using the reporter group. The method employed for detecting the reporter group depends upon the nature of the reporter group. For radioactive groups, scintillation counting or autoradiographic methods are generally appropriate. Spectroscopic methods may be used to detect dyes, luminescent groups and fluorescent groups. Biotin may be detected using avidin, coupled to a different reporter group (commonly a radioactive or fluorescent group or an enzyme). Enzyme reporter groups may generally be detected by the addition of substrate (generally for a specific period of time), followed by spectroscopic or other analysis of the reaction products.

[0642] To determine the presence or absence of a cancer, such as lung cancer, the signal detected from the reporter group that remains bound to the solid support is generally compared to a signal that corresponds to a predetermined cut-off value. In one preferred embodiment, the cut-off value for the detection of a cancer is the average mean signal obtained when the immobilized antibody is incubated with samples from patients without the cancer. In general, a sample generating a signal that is three standard deviations above the predetermined cut-off value is considered positive for the cancer. In an alternate preferred embodiment, the cut-off value is determined using a Receiver Operator Curve, according to the method of Sackett et al., Clinical Epidemiology: A Basic Science for Clinical Medicine, Little Brown and Co., 1985, p. 106-7. Briefly, in this embodiment, the cut-off value may be determined from a plot of pairs of true positive rates (i.e., sensitivity) and false positive rates (100%-specificity) that correspond to each possible cut-off value for the diagnostic test result. The cut-off value on the plot that is the closest to the upper left-hand corner (i.e., the value that encloses the largest area) is the most accurate cut-off value, and a sample generating a signal that is higher than the cut-off value determined by this method may be considered positive. Alternatively, the cut-off value may be shifted to the left along the plot, to minimize the false positive rate, or to the right, to minimize the false negative rate. In general, a sample generating a signal that is higher than the cut-off value determined by this method is considered positive for a cancer.

[0643] In a related embodiment, the assay is performed in a flow-through or strip test format, wherein the binding agent is immobilized on a membrane, such as nitrocellulose. In the flow-through test, polypeptides within the sample bind to the immobilized binding agent as the sample passes through the membrane. A second, labeled binding agent then binds to the binding agent-polypeptide complex as a solution containing the second binding agent flows through the membrane. The detection of bound second binding agent may then be performed as described above. In the strip test format, one end of the membrane to which binding agent is bound is immersed in a solution containing the sample. The sample migrates along the membrane through a region containing second binding agent and to the area of immobilized binding agent. Concentration of second binding agent at the area of immobilized antibody indicates the presence of a cancer. Typically, the concentration of second binding agent at that site generates a pattern, such as a line, that can be read visually. The absence of such a pattern indicates a negative result. In general, the amount of binding agent immobilized on the membrane is selected to generate a visually discernible pattern when the biological sample contains a level of polypeptide that would be sufficient to generate a positive signal in the two-antibody sandwich assay, in the format discussed above. Preferred binding agents for use in such assays are antibodies and antigen-binding fragments thereof. Preferably, the amount of antibody immobilized on the membrane ranges from about 25 ng to about 1 μg, and more preferably from about 50 ng to about 500 ng. Such tests can typically be performed with a very small amount of biological sample.

[0644] Of course, numerous other assay protocols exist that are suitable for use with the tumor proteins or binding agents of the present invention. The above descriptions are intended to be exemplary only. For example, it will be apparent to those of ordinary skill in the art that the above protocols may be readily modified to use tumor polypeptides to detect antibodies that bind to such polypeptides in a biological sample. The detection of such tumor protein specific antibodies may correlate with the presence of a cancer.

[0645] A cancer may also, or alternatively, be detected based on the presence of T cells that specifically react with a tumor protein in a biological sample. Within certain methods, a biological sample comprising CD4⁺ and/or CD8⁺ T cells isolated from a patient is incubated with a tumor polypeptide, a polynucleotide encoding such a polypeptide and/or an APC that expresses at least an immunogenic portion of such a polypeptide, and the presence or absence of specific activation of the T cells is detected. Suitable biological samples include, but are not limited to, isolated T cells. For example, T cells may be isolated from a patient by routine techniques (such as by Ficoll/Hypaque density gradient centrifugation of peripheral blood lymphocytes). T cells may be incubated in vitro for 2-9 days (typically 4 days) at 37° C. with polypeptide (e.g., 5-25 μg/ml). It may be desirable to incubate another aliquot of a T cell sample in the absence of tumor polypeptide to serve as a control. For CD4⁺ T cells, activation is preferably detected by evaluating proliferation of the T cells. For CD8⁺ T cells, activation is preferably detected by evaluating cytolytic activity. A level of proliferation that is at least two fold greater and/or a level of cytolytic activity that is at least 20% greater than in disease-free patients indicates the presence of a cancer in the patient.

[0646] As noted above, a cancer may also, or alternatively, be detected based on the level of mRNA encoding a tumor protein in a biological sample. For example, at least two oligonucleotide primers may be employed in a polymerase chain reaction (PCR) based assay to amplify a portion of a tumor cDNA derived from a biological sample, wherein at least one of the oligonucleotide primers is specific for (i.e., hybridizes to) a polynucleotide encoding the tumor protein. The amplified cDNA is then separated and detected using techniques well known in the art, such as gel electrophoresis. Similarly, oligonucleotide probes that specifically hybridize to a polynucleotide encoding a tumor protein may be used in a hybridization assay to detect the presence of polynucleotide encoding the tumor protein in a biological sample.

[0647] To permit hybridization under assay conditions, oligonucleotide primers and probes should comprise an oligonucleotide sequence that has at least about 60%, preferably at least about 75% and more preferably at least about 90%, identity to a portion of a polynucleotide encoding a tumor protein of the invention that is at least 10 nucleotides, and preferably at least 20 nucleotides, in length. Preferably, oligonucleotide primers and/or probes hybridize to a polynucleotide encoding a polypeptide described herein under moderately stringent conditions, as defined above. Oligonucleotide primers and/or probes which may be usefully employed in the diagnostic methods described herein preferably are at least 10-40 nucleotides in length. In a preferred embodiment, the oligonucleotide primers comprise at least 10 contiguous nucleotides, more preferably at least 15 contiguous nucleotides, of a DNA molecule having a sequence as disclosed herein. Techniques for both PCR based assays and hybridization assays are well known in the art (see, for example, Mullis et al., Cold Spring Harbor Symp. Quant. Biol., 51:263, 1987; Erlich ed., PCR Technology, Stockton Press, NY, 1989).

[0648] One preferred assay employs RT-PCR, in which PCR is applied in conjunction with reverse transcription. Typically, RNA is extracted from a biological sample, such as biopsy tissue, and is reverse transcribed to produce cDNA molecules. PCR amplification using at least one specific primer generates a cDNA molecule, which may be separated and visualized using, for example, gel electrophoresis. Amplification may be performed on biological samples taken from a test patient and from an individual who is not afflicted with a cancer. The amplification reaction may be performed on several dilutions of cDNA spanning two orders of magnitude. A two-fold or greater increase in expression in several dilutions of the test patient sample as compared to the same dilutions of the non-cancerous sample is typically considered positive.

[0649] In another embodiment, the compositions described herein may be used as markers for the progression of cancer. In this embodiment, assays as described above for the diagnosis of a cancer may be performed over time, and the change in the level of reactive polypeptide(s) or polynucleotide(s) evaluated. For example, the assays may be performed every 24-72 hours for a period of 6 months to 1 year, and thereafter performed as needed. In general, a cancer is progressing in those patients in whom the level of polypeptide or polynucleotide detected increases over time. In contrast, the cancer is not progressing when the level of reactive polypeptide or polynucleotide either remains constant or decreases with time.

[0650] Certain in vivo diagnostic assays may be performed directly on a tumor. One such assay involves contacting tumor cells with a binding agent. The bound binding agent may then be detected directly or indirectly via a reporter group. Such binding agents may also be used in histological applications. Alternatively, polynucleotide probes may be used within such applications.

[0651] As noted above, to improve sensitivity, multiple tumor protein markers may be assayed within a given sample. It will be apparent that binding agents specific for different proteins provided herein may be combined within a single assay. Further, multiple primers or probes may be used concurrently. The selection of tumor protein markers may be based on routine experiments to determine combinations that results in optimal sensitivity. In addition, or alternatively, assays for tumor proteins provided herein may be combined with assays for other known tumor antigens.

[0652] The present invention further provides kits for use within any of the above diagnostic methods. Such kits typically comprise two or more components necessary for performing a diagnostic assay. Components may be compounds, reagents, containers and/or equipment. For example, one container within a kit may contain a monoclonal antibody or fragment thereof that specifically binds to a tumor protein. Such antibodies or fragments may be provided attached to a support material, as described above. One or more additional containers may enclose elements, such as reagents or buffers, to be used in the assay. Such kits may also, or alternatively, contain a detection reagent as described above that contains a reporter group suitable for direct or indirect detection of antibody binding.

[0653] Alternatively, a kit may be designed to detect the level of mRNA encoding a tumor protein in a biological sample. Such kits generally comprise at least one oligonucleotide probe or primer, as described above, that hybridizes to a polynucleotide encoding a tumor protein. Such an oligonucleotide may be used, for example, within a PCR or hybridization assay. Additional components that may be present within such kits include a second oligonucleotide and/or a diagnostic reagent or container to facilitate the detection of a polynucleotide encoding a tumor protein.

[0654] The following Examples are offered by way of illustration and not by way of limitation.

EXAMPLES Example 1 Isolation and Characterization of cDNA Sequences Encoding Lung Tumor Polypeptides

[0655] This example illustrates the isolation of cDNA molecules encoding lung tumor-specific polypeptides from lung tumor cDNA libraries.

[0656] A. Isolation of cDNA Sequences From a Lung Squamous Cell Carcinoma Library

[0657] A human lung squamous cell carcinoma cDNA expression library was constructed from poly A⁺ RNA from a pool of two patient tissues using a Superscript Plasmid System for cDNA Synthesis and Plasmid Cloning kit (BRL Life Technologies, Gaithersburg, Md.) following the manufacturer's protocol. Specifically, lung carcinoma tissues were homogenized with polytron (Kinematica, Switzerland) and total RNA was extracted using Trizol reagent (BRL Life Technologies) as directed by the manufacturer. The poly A⁺ RNA was then purified using an oligo dT cellulose column as described in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1989. First-strand cDNA was synthesized using the NotI/Oligo-dT18 primer. Double-stranded cDNA was synthesized, ligated with BstXI/EcoRI adaptors (Invitrogen, San Diego, Calif.) and digested with NotI. Following size fractionation with cDNA size fractionation columns (BRL Life Technologies), the cDNA was ligated into the BstXI/NotI site of pcDNA3.1 (Invitrogen) and transformed into ElectroMax E. coli DH10B cells (BRL Life Technologies) by electroporation.

[0658] Using the same procedure, a normal human lung cDNA expression library was prepared from a pool of four tissue specimens. The cDNA libraries were characterized by determining the number of independent colonies, the percentage of clones that carried insert, the average insert size and by sequence analysis. The lung squamous cell carcinoma library contained 2.7×10⁶ independent colonies, with 100% of clones having an insert and the average insert size being 2100 base pairs. The normal lung cDNA library contained 1.4×10⁶ independent colonies, with 90% of clones having inserts and the average insert size being 1800 base pairs. For both libraries, sequence analysis showed that the majority of clones had a full length cDNA sequence and were synthesized from mRNA

[0659] cDNA library subtraction was performed using the above lung squamous cell carcinoma and normal lung cDNA libraries, as described by Hara et al. (Blood, 84:189-199, 1994) with some modifications. Specifically, a lung squamous cell carcinoma-specific subtracted cDNA library was generated as follows. Normal tissue cDNA library (80 μg) was digested with BamHI and XhoI, followed by a filling-in reaction with DNA polymerase Klenow fragment. After phenol-chloroform extraction and ethanol precipitation, the DNA was dissolved in 133 μl of H₂O, heat-denatured and mixed with 133 μl (133 μg) of Photoprobe biotin (Vector Laboratories, Burlingame, Calif.). As recommended by the manufacturer, the resulting mixture was irradiated with a 270 W sunlamp on ice for 20 minutes. Additional Photoprobe biotin (67 μl) was added and the biotinylation reaction was repeated. After extraction with butanol five times, the DNA was ethanol-precipitated and dissolved in 23 μl H₂O to form the driver DNA.

[0660] To form the tracer DNA, 10 μg lung squamous cell carcinoma cDNA library was digested with NotI and Spel, phenol chloroform extracted and passed through Chroma spin-400 columns (Clontech, Palo Alto, Calif.). Typically, 5 μg of cDNA was recovered after the sizing column. Following ethanol precipitation, the tracer DNA was dissolved in 5 μl H₂O. Tracer DNA was mixed with 15 μl driver DNA and 20 μl of 2×hybridization buffer (1.5 M NaCl/10 mM EDTA/50 mM HEPES pH 7.5/0.2% sodium dodecyl sulfate), overlaid with mineral oil, and heat-denatured completely. The sample was immediately transferred into a 68° C. water bath and incubated for 20 hours (long hybridization [LH]). The reaction mixture was then subjected to a streptavidin treatment followed by phenol/chloroform extraction. This process was repeated three more times. Subtracted DNA was precipitated, dissolved in 12 μl H₂O, mixed with 8 μl driver DNA and 20 μl of 2×hybridization buffer, and subjected to a hybridization at 68° C. for 2 hours (short hybridization [SH]). After removal of biotinylated double-stranded DNA, subtracted cDNA was ligated into NotI/Spel site of chloramphenicol resistant pBCSK⁺ (Stratagene, La Jolla, Calif.) and transformed into ElectroMax E. coli DH10B cells by electroporation to generate a lung squamous cell carcinoma specific subtracted cDNA library (herein after referred to as “lung subtraction I”).

[0661] A second lung squamous cell carcinoma specific subtracted cDNA library (referred to as “lung subtraction II”) was generated in a similar way to the lung subtraction library I, except that eight frequently recovered genes from lung subtraction I were included in the driver DNA, and 24,000 independent clones were recovered.

[0662] To analyze the subtracted cDNA libraries, plasmid DNA was prepared from 320 independent clones, randomly picked from the subtracted lung squamous cell carcinoma specific libraries. Representative cDNA clones were further characterized by DNA sequencing with a Perkin Elmer/Applied Biosystems Division Automated Sequencer Model 373A and/or Model 377 (Foster City, Calif.). The cDNA sequences for sixty isolated clones are provided in SEQ ID NO: 1-60. These sequences were compared to known sequences in the gene bank using the EMBL and GenBank databases (release 96). No significant homologies were found to the sequences provided in SEQ ID NO: 2, 3, 19, 38 and 46. The sequences of SEQ ID NO: 1, 6-8, 10-13, 15, 17, 18, 20-27, 29, 30, 32, 34-37, 39-45, 47-49, 51, 52, 54, 55 and 57-59 were found to show some homology to previously identified expressed sequence tags (ESTs). The sequences of SEQ ID NO: 9, 28, 31 and 33 were found to show some homology to previously identified non-human gene sequences and the sequences of SEQ ID NO: 4, 5, 14, 50, 53, 56 and 60 were found to show some homology to gene sequences previously identified in humans.

[0663] The subtraction procedure described above was repeated using the above lung squamous cell carcinoma cDNA library as the tracer DNA, and the above normal lung tissue cDNA library and a cDNA library from normal liver and heart (constructed from a pool of one sample of each tissue as described above), plus twenty other cDNA clones that were frequently recovered in lung subtractions I and II, as the driver DNA (lung subtraction III). The normal liver and heart cDNA library contained 1.76×10⁶ independent colonies, with 100% of clones having inserts and the average insert size being 1600 base pairs. Ten additional clones were isolated (SEQ ID NO: 61-70). Comparison of these cDNA sequences with those in the gene bank as described above, revealed no significant homologies to the sequences provided in SEQ ID NO: 62 and 67. The sequences of SEQ ID NO: 61, 63-66, 68 and 69 were found to show some homology to previously isolated ESTs and the sequence provided in SEQ ID NO: 70 was found to show some homology to a previously identified rat gene.

[0664] In further studies, the subtraction procedure described above was repeated using the above lung squamous cell carcinoma cDNA library as the tracer DNA, and a cDNA library from a pool of normal lung, kidney, colon, pancreas, brain, resting PBMC, heart, skin and esophagus as the driver DNA, with esophagus cDNAs making up one third of the driver material. Since esophagus is enriched in normal epithelial cells, including differentiated squamous cells, this procedure is likely to enrich genes that are tumor specific rather than tissues specific. The cDNA sequences of 48 clones determined in this subtraction are provided in SEQ ID NO: 177-224. The sequences of SEQ ID NO: 177, 178, 180, 181, 183, 187, 192, 195-197, 208, 211, 212, 215, 216, 218 and 219 showed some homology to previously identified genes. The sequences of SEQ ID NO: 179, 182, 184-186, 188-191, 193, 194, 198-207, 209 210, 213, 214, 217, 220 and 224 showed some homology to previously determined ESTs. The sequence of SEQ ID NO: 221-223 showed no homology to any previously determined sequence.

[0665] B. Isolation of cDNA Sequences From a Lung Adenocarcinoma Library

[0666] A human lung adenocarcinoma cDNA expression library was constructed as described above. The library contained 3.2×10⁶ independent colonies, with 100% of clones having an insert and the average insert size being 1500 base pairs. Library subtraction was performed as described above using the normal lung and normal liver and heart cDNA expression libraries described above as the driver DNA. Twenty-six hundred independent clones were recovered.

[0667] Initial cDNA sequence analysis from 100 independent clones revealed many ribosomal protein genes. The cDNA sequences for fifteen clones isolated in this subtraction are provided in SEQ ID NO: 71-86. Comparison of these sequences with those in the gene bank as described above revealed no significant homologies to the sequence provided in SEQ ID NO: 84. The sequences of SEQ ID NO: 71, 73, 74, 77, 78 and 80-82 were found to show some homology to previously isolated ESTs, and the sequences of SEQ ID NO: 72, 75, 76, 79, 83 and 85 were found to show some homology to previously identified human genes.

[0668] In further studies, a cDNA library (referred to as mets3616A) was constructed from a metastatic lung adenocarcinoma. The determined cDNA sequences of 25 clones sequenced at random from this library are provided in SEQ ID NO: 255-279. The mets3616A cDNA library was subtracted against a cDNA library prepared from a pool of normal lung, liver, pancreas, skin, kidney, brain and resting PBMC. To increase the specificity of the subtraction, the driver was spiked with genes that were determined to be most abundant in the mets3616A cDNA library, such as EF1-alpha, integrin-beta and anticoagulant protein PP4, as well as with cDNAs that were previously found to be differentially expressed in subtracted lung adenocarcinoma cDNA libraries. The determined cDNA sequences of 51 clones isolated from the subtracted library (referred to as mets3616A-S1) are provided in SEQ ID NO: 280-330.

[0669] Comparison of the sequences of SEQ ID NO: 255-330 with those in the public databases revealed no significant homologies to the sequences of SEQ ID NO: 255-258, 260, 262-264, 270, 272, 275, 276, 279, 281, 287, 291, 296, 300 and 310. The sequences of SEQ ID NO: 259, 261, 265-269, 271, 273, 274, 277, 278, 282-285, 288-290, 292, 294, 297-299, 301, 303-309, 313, 314, 316, 320-324 and 326-330 showed some homology to previously identified gene sequences, while the sequences of SEQ ID NO: 280, 286, 293, 302, 310, 312, 315, 317-319 and 325 showed some homology to previously isolated expressed sequence tags (ESTs).

Example 2 Determination of Tissue Specificity of Lung Tumor Polypeptides

[0670] Using gene specific primers, mRNA expression levels for seven representative lung tumor polypeptides described in Example 1 were examined in a variety of normal and tumor tissues using RT-PCR.

[0671] Briefly, total RNA was extracted from a variety of normal and tumor tissues using Trizol reagent as described above. First strand synthesis was carried out using 2 μg of total RNA with SuperScript II reverse transcriptase (BRL Life Technologies) at 42° C. for one hour. The cDNA was then amplified by PCR with gene-specific primers. To ensure the semi-quantitative nature of the RT-PCR, β-actin was used as an internal control for each of the tissues examined. 1 μl of 1:30 dilution of cDNA was employed to enable the linear range amplification of the β-actin template and was sensitive enough to reflect the differences in the initial copy numbers. Using these conditions, the β-actin levels were determined for each reverse transcription reaction from each tissue. DNA contamination was minimized by DNase treatment and by assuring a negative PCR result when using first strand cDNA that was prepared without adding reverse transcriptase.

[0672] mRNA Expression levels were examined in five different types of tumor tissue (lung squamous cell carcinoma from 3 patients, lung adenocarcinoma, colon tumor from 2 patients, breast tumor and prostate tumor), and thirteen different normal tissues (lung from 4 donors, prostate, brain, kidney, liver, ovary, skeletal muscle, skin, small intestine, stomach, myocardium, retina and testes). Using a 10-fold amount of cDNA, the antigen LST-S1-90 (SEQ ID NO: 3) was found to be expressed at high levels in lung squamous cell carcinoma and in breast tumor, and at low to undetectable levels in the other tissues examined.

[0673] The antigen LST-S2-68 (SEQ ID NO: 15) appears to be specific to lung and breast tumor, however, expression was also detected in normal kidney. Antigens LST-S1-169 (SEQ ID NO: 6) and LST-S1-133 (SEQ ID NO: 5) appear to be very abundant in lung tissues (both normal and tumor), with the expression of these two genes being decreased in most of the normal tissues tested. Both LST-S1-169 and LST-S1-133 were also expressed in breast and colon tumors. Antigens LST-S1-6 (SEQ ID NO: 7) and LST-S2-I2-5F (SEQ ID NO: 47) did not show tumor or tissue specific expression, with the expression of LST-S1-28 being rare and only detectable in a few tissues. The antigen LST-S3-7 (SEQ ID NO: 63) showed lung and breast tumor specific expression, with its message only being detected in normal testes when the PCR was performed for 30 cycles. Lower level expression was detected in some normal tissues when the cycle number was increased to 35. Antigen LST-S3-13 (SEQ ID NO: 66) was found to be expressed in 3 out of 4 lung tumors, one breast tumor and both colon tumor samples. Its expression in normal tissues was lower compared to tumors, and was only detected in 1 out of 4 normal lung tissues and in normal tissues from kidney, ovary and retina. Expression of antigens LST-S3-4 (SEQ ID NO: 62) and LST-S3-14 (SEQ ID NO: 67) was rare and did not show any tissue or tumor specificity. Consistent with Northern blot analyses, the RT-PCR results on antigen LAT-S1-A-10A (SEQ ID NO: 78) suggested that its expression is high in lung, colon, stomach and small intestine tissues, including lung and colon tumors, whereas its expression was low or undetectable in other tissues.

[0674] A total of 2002 cDNA fragments isolated in lung subtractions I, II and III, described above, were colony PCR amplified and their mRNA expression levels in lung tumor, normal lung, and various other normal and tumor tissues were determined using microarray technology (Synteni, Palo Alto, Calif.). Briefly, the PCR amplification products were dotted onto slides in an array format, with each product occupying a unique location in the array. mRNA was extracted from the tissue sample to be tested, reverse transcribed, and fluorescent-labeled cDNA probes were generated. The microarrays were probed with the labeled cDNA probes, the slides scanned and fluorescence intensity was measured. This intensity correlates with the hybridization intensity. Seventeen non-redundant cDNA clones showed over-expression in lung squamous tumors, with expression in normal tissues tested (lung, skin, lymph node, colon, liver, pancreas, breast, heart, bone marrow, large intestine, kidney, stomach, brain, small intestine, bladder and salivary gland) being either undetectable, or 10-fold less compared to lung squamous tumors. The determined cDNA sequences for the clone L513S are provided in SEQ ID NO: 87 and 88; those for L514S are provided in SEQ ID NO: 89 and 90; those for L516S in SEQ ID NO: 91 and 92; that for L517S in SEQ ID NO: 93; that for L519S in SEQ ID NO: 94; those for L520S in SEQ ID NO: 95 and 96; those for L521S in SEQ ID NO: 97 and 98; that for L522S in SEQ ID NO: 99; that for L523S in SEQ ID NO: 100; that for L524S in SEQ ID NO: 101; that for L525S in SEQ ID NO: 102; that for L526S in SEQ ID NO: 103; that for L527S in SEQ ID NO: 104; that for L528S in SEQ ID NO: 105; that for L529S in SEQ ID NO: 106; and those for L530S in SEQ ID NO: 107 and 108. Additionally, the full-length cDNA sequence for L530S is provided in SEQ ID NO: 151, with the corresponding amino acid sequence being provided in SEQ ID NO: 152. L530S shows homology to a splice variant of a p53 tumor suppressor homologue, p63. The cDNA sequences of 7 known isoforms of p63 are provided in SEQ ID NO: 331-337, with the corresponding amino acid sequences being provided in SEQ ID NO: 338-344, respectively.

[0675] Due to polymorphisms, the clone L531S appears to have two forms. A first determined full-length cDNA sequence for L531S is provided in SEQ ID NO: 109, with the corresponding amino acid sequence being provided in SEQ ID NO: 110. A second determined full-length cDNA sequence for L531S is provided in SEQ ID NO: 111, with the corresponding amino acid sequence being provided in SEQ ID NO: 112. The sequence of SEQ ID NO: 1 is identical to that of SEQ ID NO: 109, except that it contains a 27 bp insertion. Similarly, L514S has two alternatively spliced forms; the first variant cDNA is listed as SEQ ID NO: 153, with the corresponding amino acid sequence being provided in SEQ ID NO: 155. The full-length cDNA for the second variant form of L514S is provided in SEQ ID NO: 154, with the corresponding amino acid sequence being provided in SEQ ID NO: 156.

[0676] Full length cloning for L524S (SEQ ID NO: 101) yielded two variants (SEQ ID NO: 163 and 164) with the corresponding amino acid sequences of SEQ ID NO: 165 and 166, respectively. Both variants have been shown to encode parathyroid hormone-related peptide.

[0677] Attempts to isolate the full-length cDNA for L519S, resulted in the isolation of the extended cDNA sequence provided in SEQ ID NO: 173, which contains a potential open reading frame. The amino acid sequence encoded by the sequence of SEQ ID NO: 173 is provided in SEQ ID NO: 174. Additionally, the full-length cDNA sequence for the clone of SEQ ID NO: 100 (known as L523S), a known gene, is provided in SEQ ID NO: 175, with the corresponding amino acid sequence being provided in SEQ ID NO: 176. In further studies, a full-length cDNA sequence for L523S was isolated from a L523S-positive tumor cDNA library by PCR amplification using gene specific primers designed from the sequence of SEQ ID NO: 175. The determined full-length cDNA sequence is provided in SEQ ID NO: 347. The amino acid sequence encoded by this sequence is provided in SEQ ID NO: 348. This protein sequence differs from the previously published protein sequence at two amino acid positions, namely at positions 158 and 410.

[0678] Comparison of the sequences of L514S and L531S (SEQ ID NO: 87 and 88, and 109, respectively) with those in the gene bank, as described above, revealed no significant homologies to known sequences. The sequences of L513S, L516S, L517S, L519S, L520S and L530S (SEQ ID NO: 87 and 88, 91 and 92, 93, 94, 95 and 96, 107 and 108, respectively) were found to show some homology to previously identified ESTs. The sequences of L521S, L522S, L523S, L524S, L525S, L526S, L527S, L528S and L529S (SEQ ID NO: 97 and 98, 99, 99, 101, 102, 103, 104, 105, and 106, respectively) were found to represent known genes. The determined full-length cDNA sequence for L520S is provided in SEQ ID NO: 113, with the corresponding amino acid sequence being provided in SEQ ID NO: 114. Subsequent microarray analysis showed L520S to be overexpressed in breast tumors in addition to lung squamous tumors.

[0679] Further analysis demonstrated that L529S (SEQ ID NO: 106 and 115), L525S (SEQ ID NO: 102 and 120) and L527S (SEQ ID NO: 104) are cytoskeletal components and potentially squamous cell specific proteins. L529S is connexin 26, a gap junction protein. It was found to be highly expressed in one lung squamous tumor, referred to as 9688T, and moderately over-expressed in two others. However, lower level expression of connexin 26 is also detectable in normal skin, colon, liver and stomach. The over-expression of connexin 26 in some breast tumors has been reported and a mutated form of L529S may result in over-expression in lung tumors. L525S is plakophilin 1, a desmosomal protein found in plaque-bearing adhering junctions of the skin. Expression levels for L525S mRNA was highly elevated in three out of four lung squamous tumors tested, and in normal skin. L527S has been identified as keratin 6 isoform, type II 58 Kd keratin and cytokeratin 13, and shows over-expression in squamous tumors and low expression in normal skin, breast and colon tissues. Keratin and keratin-related genes have been extensively documented as potential markers for lung cancer including CYFRA2.1 (Pastor, A., et al, Eur. Respir. J., 10:603-609, 1997). L513S (SEQ ID NO: 87 and 88) shows moderate over-expression in several tumor tissues tested, and encodes a protein that was first isolated as a pemphigus vulgaris antigen.

[0680] L520S (SEQ ID NO: 95 and 96) and L521S (SEQ ID NO: 97 and 98) are highly expressed in lung squamous tumors, with L520S being up-regulated in normal salivary gland and L521S being over-expressed in normal skin. Both belong to a family of small proline rich proteins and represent markers for fully differentiated squamous cells. L521S has been described as a specific marker for lung squamous tumor (Hu, R., et al, Lung Cancer, 20:25-30, 1998). L515S (SEQ ID NO: 162) encodes IGF-β2 and L516S is an aldose reductase homologue. Both are moderately expressed in lung squamous tumors and in normal colon. Notably, L516S (SEQ ID NO: 91 and 92) is up-regulated in metastatic tumors but not primary lung adenocarcinoma, an indication of its potential role in metatasis and a potential prognostic marker. L522S (SEQ ID NO: 99) is moderately over-expressed in lung squamous tumors with minimum expression in normal tissues. L522S has been shown to belong to a class IV alcohol dehydrogenase, ADH7, and its expression profile suggests it is a squamous cell specific antigen. L523S (SEQ ID NO: 100) is moderately over-expressed in lung squamous tumor, human pancreatic cancer cell lines and pancreatic cancer tissues, suggesting this gene may be a shared antigen between pancreatic and lung squamous cell cancer.

[0681] L524S (SEQ ID NO: 101) is over-expressed in the majority of squamous tumors tested and is homologous with parathyroid hormone-related peptide (PTHrP), which is best known to cause humoral hypercalcaemia associated with malignant tumors such as leukemia, prostate and breast cancer. It is also believed that PTHrP is most commonly associated with squamous carcinoma of lung and rarely with lung adenocarcinoma (Davidson, L. A., et al, J. Pathol., 178: 398-401, 1996). L528S (SEQ ID NO: 105) is highly over-expressed in two lung squamous tumors with moderate expression in two other squamous tumors, one lung adenocarcinoma and some normal tissues, including skin, lymph nodes, heart, stomach and lung. It encodes the NMB gene that is similar to the precursor of melanocyte specific gene Pmel17, which is reported to be preferentially expressed in low-metastatic potential melanoma cell lines. This suggests that L528S may be a shared antigen in both melanoma and lung squamous cell carcinoma. L526S (SEQ ID NO: 103) was overexpressed in all lung squamous cell tumor tissues tested and has been shown to share homology with a gene (ATM) in which a mutation causes ataxia telangiectasia, a genetic disorder in humans causing a predisposition to cancer, among other symptoms. ATM encodes a protein that activates a p53 mediated cell-cycle checkpoint through direct binding and phosphorylation of the p53 molecule. Approximately 40% of lung cancers are associated with p53 mutations, and it is speculated that over-expression of ATM is a result of compensation for loss of p53 function, but it is unknown whether over-expression is the cause of result of lung squamous cell carcinoma. Additionally, expression of L526S (ATM) is also detected in a metastatic but not lung adenocarcinoma, suggesting a role in metastasis.

[0682] Expression of L523S (SEQ ID NO: 175), was examined by real time RT-PCR as described above. In a first study using a panel of lung squamous tumors, L523S was found to be expressed in 4/7 lung squamous tumors, 2/3 head and neck squamous tumors and 2/2 lung adenocarcinomas, with low level expression being observed in skeletal muscle, soft palate and tonsil. In a second study using a lung adenocarcinoma panel, expression of L523S was observed in 4/9 primary adenocarcinomas, 2/2 lung pleural effusions, 1/1 metastatic lung adenocarcinomas and 2/2 lung squamous tumors, with little expression being observed in normal tissues.

[0683] Expression of L523S in lung tumors and various normal tissues was also examined by Northern blot analysis, using standard techniques. In a first study, L523S was found to be expressed in a number of lung adenocarcinomas and squamous cell carcinomas, as well as normal tonsil. No expression was observed in normal lung. In a second study using a normal tissue blot (referred to as HB-12) from Clontech, no expression was observed in brain, skeletal muscle, colon, thymus, spleen, kidney, liver, small intestine, lung or PBMC, although there was strong expression in placenta.

Example 3 Isolation and Characterization of Lung Tumor Polypeptides by PCR-Based Subtraction

[0684] Eight hundred and fifty seven clones from a cDNA subtraction library, containing cDNA from a pool of two human lung squamous tumors subtracted against eight normal human tissue cDNAs including lung, PBMC, brain, heart, kidney, liver, pancreas, and skin, (Clontech, Palo Alto, Calif.) were derived and submitted to a first round of PCR amplification. This library was subjected to a second round of PCR amplification, following the manufacturer's protocol. The resulting cDNA fragments were subcloned into the P7-Adv vector (Clontech, Palo Alto, Calif.) and transformed into DH5α E. coli (Gibco, BRL). DNA was isolated from independent clones and sequenced using a Perkin Elmer/Applied Biosystems Division Automated Sequencer Model 373A.

[0685] One hundred and sixty two positive clones were sequenced. Comparison of the DNA sequences of these clones with those in the EMBL and GenBank databases, as described above, revealed no significant homologies to 13 of these clones, hereinafter referred to as Contigs 13, 16, 17, 19, 22, 24, 29, 47, 49, 56-59. The determined cDNA sequences for these clones are provided in SEQ ID NO: 125, 127-129, 131-133, 142, 144, 148-150, and 157, respectively. Contigs 1, 3-5, 7-10, 12, 11, 15, 20, 31, 33, 38, 39, 41, 43, 44, 45, 48, 50, 53, 54 (SEQ ID NO: 115-124, 126, 130, 134-141, 143, 145-147, respectively) were found to show some degree of homology to previously identified DNA sequences. Contig 57 (SEQ ID NO: 149) was found to represent the clone L519S (SEQ ID NO: 94) disclosed in U.S. patent application Ser. No. 09/123,912, filed Jul. 27, 1998. To the best of the inventors' knowledge, none of these sequences have been previously shown to be differentially over-expressed in lung tumors.

[0686] mRNA expression levels for representative clones in lung tumor tissues, normal lung tissues (n=4), resting PBMC, salivary gland, heart, stomach, lymph nodes, skeletal muscle, soft palate, small intestine, large intestine, bronchial, bladder, tonsil, kidney, esophagus, bone marrow, colon, adrenal gland, pancreas, and skin (all derived from human) were determined by RT-PCR as described above. Expression levels using microarray technology, as described above, were examined in one sample of each tissue type unless otherwise indicated.

[0687] Contig 3 (SEQ ID NO: 116) was found to be highly expressed in all head and neck squamous cell tumors tested (17/17), and expressed in the majority (8/12) of lung squamous tumors, (high expression in 7/12, moderate in 2/12, and low in 2/12), while showing negative expression for 2/4 normal lung tissues and low expression in the remaining two samples. Contig 3 showed moderate expression in skin and soft palate, and lowered expression levels in resting PBMC, large intestine, salivary gland, tonsil, pancreas, esophagus, and colon. Contig 11 (SEQ ID NO: 124) was found to be expressed in all head and neck squamous cell tumors tested (17/17), with high levels of expression being seen in 14/17 tumors, and moderately levels of expression being seen in 3/17 tumors. Additionally, high expression was seen in 3/12 lung squamous tumors and moderate expression in 4/12 lung squamous tumors. Contig 11 was negative for 3/4 normal lung samples, with the remaining sample having only low expression. Contig 11 showed low to moderate reactivity to salivary gland, soft palate, bladder, tonsil, skin, esophagus, and large intestine. Contig 13 (SEQ ID NO: 125) was found to be expressed in all head and neck squamous cell tumors tested (17/17), with high expression in 12/17, and moderate expression in 5/17. Contig 13 was expressed in 7/12 lung squamous tumors, with high expression in 4/12 and moderate expression in three samples. Analysis of normal lung samples showed negative expression for 2/4 and low to moderate expression in the remaining two samples. Contig 13 showed low to moderate reactivity to resting PBMC, salivary gland, bladder, pancreas, tonsil, skin, esophagus, and large intestine, as well as high expression in soft palate. Subsequent full-length cloning efforts revealed that contig 13 (also known as L761P) maps to the 3′ untranslated region of the hSec10p gene. The full-length sequence for this gene is set forth in SEQ ID NO: 368, and encodes the protein set forth in SEQ ID NO: 369.

[0688] Contig 16 (SEQ ID NO: 127) was found to be moderately expressed in several head and neck squamous cell tumors (6/17) and one lung squamous tumor, while showing no expression in any normal lung samples tested. Contig 16 showed low reactivity to resting PBMC, large intestine, skin, salivary gland, and soft palate. Contig 17 (SEQ ID NO: 128) was shown to be expressed in all head and neck squamous cell tumors tested (17/17) (highly expressed in 5/17, and moderately expressed in 12/17). Determination of expression levels in lung squamous tumors showed one tumor sample with high expression and 3/12 with moderate levels. Contig 17 was negative for 2/4 normal lung samples, with the remaining samples having only low expression. Additionally, low level expression was found in esophagus and soft palate. Contig 19 (SEQ ID NO: 129) was found to be expressed in most head and neck squamous cell tumors tested (11/17); with two samples having high expression levels, 6/17 showing moderate expression, and low expression being found in 3/17. Testing in lung squamous tumors revealed only moderate expression in 3/12 samples. Expression levels in 2/4 of normal lung samples were negative, the two other samples having only low expression. Contig 19 showed low expression levels in esophagus, resting PBMC, salivary gland, bladder, soft palate and pancreas.

[0689] Contig 22 (SEQ ID NO: 131), was shown to be expressed in most head and neck squamous cell tumors tested (13/17) with high expression in four of these samples, moderate expression in 6/17, and low expression in 3/17. Expression levels in lung squamous tumors were found to be moderate to high for 3/12 tissues tested, with negative expression in two normal lung samples and low expression in two other samples (n=4). Contig 22 showed low expression in skin, salivary gland and soft palate. Similarly, Contig 24 (SEQ ID NO: 132) was found to be expressed in most head and neck squamous cell tumors tested (13/17) with high expression in three of these samples, moderate expression in 6/17, and low expression in 4/17. Expression levels in lung squamous tumors were found to be moderate to high for 3/12 tissues tested, with negative expression for three normal lung samples and low expression in one sample (n=4). Contig 24 showed low expression in skin, salivary gland and soft palate. Contig 29 (SEQ ID NO: 133) was expressed in nearly all head and neck squamous cell tumors tested (16/17): highly expressed in 4/17, moderately expressed in 11/17, with low expression in one sample. Also, it was moderately expressed in 3/12 lung squamous tumors, while being negative for 2/4 normal lung samples. Contig 29 showed low to moderate expression in large intestine, skin, salivary gland, pancreas, tonsil, heart and soft palate. Contig 47 (SEQ ID NO: 142) was expressed in most head and neck squamous cell tumors tested (12/17): moderate expression in 10/17, and low expression in two samples. In lung squamous tumors, it was highly expressed in one sample and moderately expressed in two others (n=1 3). Contig 47 was negative for 2/4 normal lung samples, with the remaining two samples having moderate expression. Also, Contig 47 showed moderate expression in large intestine, and pancreas, and low expression in skin, salivary gland, soft palate, stomach, bladder, resting PBMC, and tonsil.

[0690] Contig 48 (SEQ ID NO: 143) was expressed in all head and neck squamous cell tumors tested (17/17): highly expressed in 8/17 and moderately expressed in 7/17, with low expression in two samples. Expression levels in lung squamous tumors were high to moderate in three samples (n=13). Contig 48 was negative for one out of four normal lung samples, the remaining showing low or moderate expression. Contig 48 showed moderate expression in soft palate, large intestine, pancreas, and bladder, and low expression in esophagus, salivary gland, resting PBMC, and heart. Contig 49 (SEQ ID NO: 144) was expressed at low to moderate levels in 6/17 head and neck squamous cell tumors tested. Expression levels in lung squamous tumors were moderate in three samples (n=13). Contig 49 was negative for 2/4 normal lung samples, the remaining samples showing low expression. Moderate expression levels in skin, salivary gland, large intestine, pancreas, bladder and resting PBMC were shown, as well as low expression in soft palate, lymph nodes, and tonsil. Contig 56 (SEQ ID NO: 148) was expressed in low to moderate levels in 3/17 head and neck squamous cell tumors tested, and in lung squamous tumors, showing low to moderate levels in three out of thirteen samples. Notably, low expression levels were detected in one adenocarcinoma lung tumor sample (n=2). Contig 56 was negative for 3/4 normal lung samples, and showed moderate expression levels in only large intestine, and low expression in salivary gland, soft palate, pancreas, bladder, and resting PBMC. Contig 58, also known as L769P, (SEQ ID NO: 150) was expressed at moderate levels in 11/17 head and neck squamous cell tumors tested and low expression in one additional sample. Expression in lung squamous tumors showed low to moderate levels in three out of thirteen samples. Contig 58 was negative for 3/4 normal lung samples, with one sample having low expression. Moderate expression levels in skin, large intestine, and resting PBMC were demonstrated, as well as low expression in salivary gland, soft palate, pancreas, and bladder. Contig 59 (SEQ ID NO: 157) was expressed in some head, neck, and lung squamous tumors. Low level expression of Contig 59 was also detected in salivary gland and large intestine.

[0691] The full-length cDNA sequence for Contig 22, also referred to as L763P, is provided in SEQ ID NO: 158, with the corresponding amino acid sequence being provided in SEQ ID NO: 159. Real-time RT-PCR analysis of L763P revealed that it is highly expressed in 3/4 lung squamous tumors as well as 4/4 head and neck squamous tumors, with low level expression being observed in normal brain, skin, soft pallet and trachea. Subsequent database searches revealed that the sequence of SEQ ID NO: 158 contains a mutation, resulting in a frameshift in the corresponding protein sequence. A second cDNA sequence for L763P is provided in SEQ ID NO: 345, with the corresponding amino acid sequence being provided in SEQ ID NO: 346. The sequences of SEQ ID NO: 159 and 346 are identical with the exception of the C-terminal 33 amino acids of SEQ ID NO: 159.

[0692] The full-length cDNA sequence incorporating Contigs 17, 19, and 24, referred to as L762P, is provided in SEQ ID NO: 160, with the corresponding amino acid sequence being provided in SEQ ID NO: 161. Further analysis of L762P has determined it to be a type I membrane protein and two additional variants have been sequenced. Variant 1 (SEQ ID NO: 167, with the corresponding amino acid sequence in SEQ ID NO: 169) is an alternatively spliced form of SEQ ID NO: 160 resulting in deletion of 503 nucleotides, as well as deletion of a short segment of the expressed protein. Variant 2 (SEQ ID NO: 168, with the corresponding amino acid sequence in SEQ ID NO: 170) has a two nucleotide deletion at the 3′ coding region in comparison to SEQ ID NO: 160, resulting in a secreted form of the expressed protein. Real-time RT-PCR analysis of L762P revealed that is over-expressed in 3/4 lung squamous tumors and 4/4 head & neck tumors, with low level expression being observed in normal skin, soft pallet and trachea.

[0693] An epitope of L762P was identified as having the sequence KPGHWTYTLNNTHHSLQALK (SEQ ID NO: 382), which corresponds to amino acids 571-590 of SEQ ID NO: 161.

[0694] The full-length cDNA sequence for contig 56 (SEQ ID NO: 148), also referred to as L773P, is provided in SEQ ID NO: 171, with the amino acid sequence in SEQ ID NO: 172. L773P was found to be identical to dihydroxyl dehydrogenase at the 3′ portion of the gene, with divergent 5′ sequence. As a result, the 69 N-terminal amino acids are unique. The cDNA sequence encoding the 69 N-terminal amino acids is provided in SEQ ID NO: 349, with the N-terminal amino acid sequence being provided in SEQ ID NO: 350. Real-time PCR revealed that L773P is highly expressed in lung squamous tumor and lung adenocarcinoma, with no detectable expression in normal tissues. Subsequent Northern blot analysis of L773P demonstrated that this transcript is differentially over-expressed in squamous tumors and detected at approximately 1.6 Kb in primary lung tumor tissue and approximately 1.3 Kb in primary head and neck tumor tissue.

[0695] Subsequent microarray analysis has shown Contig 58, also referred to as L769S (SEQ ID NO: 150), to be overexpressed in breast tumors in addition to lung squamous tumors.

Example 4 Isolation and Characterization of Lung Tumor Polypeptides by PCR-Based Subtraction

[0696] Seven hundred and sixty clones from a cDNA subtraction library, containing cDNA from a pool of two human lung primary adenocarcinomas subtracted against a pool of nine normal human tissue cDNAs including skin, colon, lung, esophagus, brain, kidney, spleen, pancreas and liver, (Clontech, Palo Alto, Calif.) were derived and submitted to a first round of PCR amplification. This library (referred to as ALT-1) was subjected to a second round of PCR amplification, following the manufacturer's protocol. The expression levels of these 760 cDNA clones in lung tumor, normal lung, and various other normal and tumor tissues, were examined using microarray technology (Incyte, Palo Alto, Calif.). Briefly, the PCR amplification products were dotted onto slides in an array format, with each product occupying a unique location in the array. mRNA was extracted from the tissue sample to be tested, reverse transcribed, and fluorescent-labeled cDNA probes were generated. The microarrays were probed with the labeled cDNA probes, the slides scanned and fluorescence intensity was measured. This intensity correlates with the hybridization intensity. A total of 118 clones, of which 55 were unique, were found to be over-expressed in lung tumor tissue, with expression in normal tissues tested (lung, skin, lymph node, colon, liver, pancreas, breast, heart, bone marrow, large intestine, kidney, stomach, brain, small intestine, bladder and salivary gland) being either undetectable, or at significantly lower levels. One of these clones, having the sequence as provided in SEQ ID NO: 420 (clone #19014), shows homology to a previously identified clone, L773P. Clone L773P has the full-length cDNA sequence provided in SEQ ID NO: 171 and the amino acid sequence provided in SEQ ID NO: 172 The isolation of clone #19014 is also described in co-pending U.S. patent application Ser. No. 09/285,479, filed Apr. 2, 1999.

Example 5 Synthesis of Polypeptides

[0697] Polypeptides may be synthesized on a Perkin Elmer/Applied Biosystems Division 430A peptide synthesizer using FMOC chemistry with HPTU (0-Benzotriazole-N,N,N′,N′-tetramethyluronium hexafluorophosphate) activation. A Gly-Cys-Gly sequence may be attached to the amino terminus of the peptide to provide a method of conjugation, binding to an immobilized surface, or labeling of the peptide. Cleavage of the peptides from the solid support may be carried out using the following cleavage mixture: trifluoroacetic acid:ethanedithiol:thioanisole:water:phenol (40:1:2:2:3). After cleaving for 2 hours, the peptides may be precipitated in cold methyl-t-butyl-ether. The peptide pellets may then be dissolved in water containing 0.1% trifluoroacetic acid (TFA) and lyophilized prior to purification by C18 reverse phase HPLC. A gradient of 0%-60% acetonitrile (containing 0.1% TFA) in water (containing 0.1% TFA) may be used to elute the peptides. Following lyophilization of the pure fractions, the peptides may be characterized using electrospray or other types of mass spectrometry and by amino acid analysis.

Example 6 Preparation of Antibodies Against Lung Cancer Antigens

[0698] Polyclonal antibodies against the lung cancer antigens L514S, L528S, L531S, L523 and L773P (SEQ ID NO: 155, 225, 112, 176 and 171, respectively) were prepared as follows.

[0699] Rabbits were immunized with recombinant protein expressed in and purified from E. coli as described below. For the initial immunization, 400 μg of antigen combined with muramyl dipeptide (MDP) was injected subcutaneously (S.C.). Animals were boosted S.C. 4 weeks later with 200 μg of antigen mixed with incomplete Freund's Adjuvant (IFA). Subsequent boosts of 100 μg of antigen mixed with IFA were injected S.C. as necessary to induce high antibody titer responses. Serum bleeds from immunized rabbits were tested for antigen-specific reactivity using ELISA assays with purified protein. Polyclonal antibodies against L514S, L528S, L531S, L523S and L773P were affinity purified from high titer polyclonal sera using purified protein attached to a solid support.

[0700] Immunohistochemical analysis using polyclonal antibodies against L514S was performed on a panel of 5 lung tumor samples, 5 normal lung tissue samples and normal colon, kidney, liver, brain and bone marrow. Specifically, tissue samples were fixed in formalin solution for 24 hours and embedded in paraffin before being sliced into 10 micron sections. Tissue sections were permeabilized and incubated with antibody for 1 hr. HRP-labeled anti-mouse followed by incubation with DAB chromogen was used to visualize L514S immunoreactivity. L514S was found to be highly expressed in lung tumor tissue with little or no expression being observed in normal lung, brain or bone marrow. Light staining was observed in colon (epithelial crypt cells positive) and kidney (tubules positive). Staining was seen in normal liver but no mRNA has been detected in this tissue making this result suspect.

[0701] Using the same procedure, immunohistochemical analysis using polyclonal antibodies against L528S demonstrated staining in lung tumor and normal lung samples, light staining in colon and kidney, and no staining in liver and heart.

[0702] Immunohistochemical analysis using polyclonal antibodies against L531S demonstrated staining in lung tumor samples, light membrane staining in most normal lung samples, epithelial staining in colon, tubule staining in kidney, ductal epithelial staining in liver and no staining in heart.

[0703] Immunohistochemical analysis using polyclonal antibodies against L523S demonstrated staining in all lung cancer samples tested but no staining in normal lung, kidney, liver, colon, bone marrow or cerebellum.

[0704] Generation of polyclonal anti-sera against L762P (SEQ ID NO: 169 and 170) was performed as follows. 400 micrograms of lung antigen was combined with 100 micrograms of muramyldipeptide (MDP). An equal volume of Incomplete Freund's Adjuvant (IFA) was added and then mixed until an emulsion was formed. Rabbits were injected subcutaneously (S.C.). After four weeks the animals were injected S.C. with 200 micrograms of antigen mixed with an equal volume of IFA. Every four weeks animals were boosted with 100 micrograms of antigen. Seven days following each boost the animal was bled. Sera was generated by incubating the blood at 4° C. for 12-24 hours followed by centrifugation.

[0705] Characterization of polyclonal antisera was carried out as follows. Ninety-six well plates were coated with antigen by incubing with 50 microliters (typically 1 microgram) at 4° C. for 20 hrs. 250 microliters of BSA blocking buffer was added to the wells and incubated at room temperature for 2 hrs. Plates were washed 6 times with PBS/0.01% Tween. Rabbit sera was diluted in PBSand 50 microliters of diluted sera was added to each well and incubated at room temperature for 30 min. Plates were washed as described above before addition of 50 microliters of goat anti-rabbit horse radish peroxidase (HRP) at a 1:10000 dilution and incubation at room temperature for 30 min. Plates were washed as described above and 100 μl of TMB Microwell Peroxidase Substrate was added to each well. Following a 15 minute incubation in the dark at room temperature, the calorimetric reaction was stopped with 100 μl 1N H₂SO₄ and read immediately at 450 nm. Antisera showed strong reactivity to antigen L762P.

[0706] Immunohistochemical analysis using polyclonal antibodies against L762P demonstrated staining in all lung cancer samples tested, some light staining in the bronchiole epithelium of normal lung, tubule staining in kidney, light epithelial staining in colon and no staining in heart or liver.

[0707] In order to evaluate L773P protein expression in various tissues, immunohistochemistry (IHC) analysis was performed using an affinity purified L773P polyclonal antibody. Briefly, tissue samples were fixed in formalin solution for 12-24 hrs and embedded in paraffin before being sliced into 8 micron sections. Steam heat induced epitope retrieval (SHIER) in 0.1 M sodiuym citrate buffer (pH 6.0) was used for optimal staining conditions. Sections were incubated with 10% serum/PBS for 5 minutes. Primary antibody was added to each section for 25 minutes at indicated concentrations followed by 25 minute incubation with either anti-rabbit or anti-mouse biotinylated antibody. Endogenous peroxidase activitiy was blocked by three 1.5 minute incubations with hydrogen peroxidase. The avidin biotin complex/horse radish peroxidase (ABC/HRP) system was used along with DAB chromogen to visualize L773P expression. Slides were counterstained with hematoxylin to visualize cell nuclei. Using this approach, L773P protein was detected in 6/8 lung tumors, 4/6 normal lung samples (very light staining in some cases), 1/1 kidney samples (very light staining), 0/1 heart samples, 1/1 colon samples (very light staining) and 0/1 liver samples.

Example 7 Peptide Priming of Mice and Propagation of CTL Lines

[0708] Immunogenic peptides from the lung cancer antigen L762P (SEQ ID NO: 161) for HLA-A2/K^(b)-resticted CD8+ T cells were identified as follows.

[0709] The location of HLA-A2 binding peptides within the lung cancer antigen L762P (SEQ ID NO: 161) was predicted using a computer program which predicts peptides sequences likely to being to HLA-A*0201 by fitting to the known peptide binding motif for HLA-A*0201 (Rupert et al. (1993) Cell 74:929; Rammensee et al. (1995) Immunogenetics 41:178-228). A series of 19 synthetic peptides corresponding to a selected subset of the predicted HLA-A*0201 binding peptides was prepared as described above.

[0710] Mice expressing the transgene for human HLA A2/Kb (provided by Dr L. Sherman, The Scripps Research Institute, La Jolla, Calif.) were immunized with the synthetic peptides, as described by Theobald et al., Proc. Natl. Acad Sci. USA 92:11993-11997, 1995, with the following modifications. Mice were immunized with 50 μg of L726P peptide and 120 μg of an I-A^(b) binding peptide derived from hepatitis B virus protein emulsified in incomplete Freund's adjuvant. Three weeks later these mice were sacrificed and single cell suspensions prepared. Cells were then resuspended at 7×10⁶ cells/ml in complete media (RPMI-1640; Gibco BRL, Gaithersburg, Md.) containing 10% FCS, 2 mM Glutamine (Gibco BRL), sodium pyruvate (Gibco BRL), non-essential amino acids (Gibco BRL), 2×10⁻⁵ M 2-mercaptoethanol, 50 U/ml penicillin and streptomycin, and cultured in the presence of irradiated (3000 rads) L762P peptide-(5 μg/ml) and 10 mg/ml B₂-microglobulin-(3 μg/ml) LPS blasts (A2 transgenic spleens cells cultured in the presence of 7 μg/ml dextran sulfate and 25 μg/ml LPS for 3 days). After six days, cells (5×10⁵/ml) were restimulated with 2.5×10⁶/ml peptide-pulsed irradiated (20,000 rads) EL4A2Kb cells (Sherman et al, Science 258:815-818, 1992) and 5×10⁶/ml irradiated (3000 rads) A2/K^(b)-transgenic spleen feeder cells. Cells were cultured in the presence of 10 U/ml IL-2. Cells were restimulated on a weekly basis as described, in preparation for cloning the line.

[0711] Peptide-specific cell lines were cloned by limiting dilution analysis with irradiated (20,000 rads) L762P peptide-pulsed EL4 A2Kb tumor cells (1×10⁴ cells/well) as stimulators and irradiated (3000 rads) A2/K^(b)-transgenic spleen cells as feeders (5×10⁵ cells/ well) grown in the presence of 10 U/ml IL-2. On day 7, cells were restimulated as before. On day 14, clones that were growing were isolated and maintained in culture.

[0712] Cell lines specific for the peptides L762P-87 (SEQ ID NO: 226; corresponding to amino acids 87-95 of SEQ ID NO: 161), L762P-145 (SEQ ID NO: 227; corresponding to amino acids 145-153 of SEQ ID NO: 161), L762P-585 (SEQ ID NO: 228; corresponding to amino acids 585-593 of SEQ ID NO: 161), L762P-425 (SEQ ID NO: 229; corresponding to amino acids 425-433 of SEQ ID NO: 161), L762P(10)-424 (SEQ ID NO: 230; corresponding to amino acids 424-433 of SEQ ID NO: 161) and L762P(10)-458 (SEQ ID NO: 231; corresponding to amino acids 458-467 of SEQ ID NO: 161) demonstrated significantly higher reactivity (as measured by percent specific lysis) against L762P peptide-pulsed EL4-A2/K^(b) tumor target cells than control peptide-pulsed EL4-A2/K^(b) tumor target cells.

Example 8 Identication of CD4 Immunogenic T Cell Epitopes Derived From The Lung Cancer Antigen L762P

[0713] CD4 T cell lines specific for the antigen L762P (SEQ ID NO: 161) were generated as follows.

[0714] A series of 28 overlapping peptides were synthesized that spanned approximately 50% of the L762P sequence. For priming, peptides were combined into pools of 4-5 peptides, pulsed at 20 micrograms/ml into dendritic cells for 24 hours. The dendritic cells were then washed and mixed with positively selected CD4+ T cells in 96 well U-bottomed plates. Forty cultures were generated for each peptide pool. Cultures were restimulated weekly with fresh dendritic cells loaded with peptide pools. Following a total of 3 stimulation cycles, cells were rested for an additional week and tested for specificity to antigen presenting cells (APC) pulsed with peptide pools using interferon-gamma ELISA and proliferation assays. For these assays, adherent monocytes loaded with either the relevant peptide pool or an irrelevant peptide were used as APC. T cell lines that appeared to specifically recognize L762P peptide pools both by cytokine release and proliferation were identified for each pool. Emphasis was placed on identifying T cells with proliferative responses. T cell lines that demonstrated either both L762P-specific cytokine secretion and proliferation, or strong proliferation alone were further expanded to be tested for recognition of individual peptides from the pools, as well as for recognition of recombinant L762P. The source of recombinant L762P was E. coli, and the material was partially purified and endotoxin positive. These studies employed 10 micrograms of individual peptides, 10 or 2 micrograms of an irrelevant peptide, and 2 or 0.5 micrograms of either L762P protein or an irrelevant, equally impure, E. coli generated recombinant protein. Significant interferon-gamma production and CD4 T cell proliferation was induced by a number of L762P-derived peptides in each pool. The amino acid sequences for these peptides are provided in SEQ ID NO: 232-251. These peptides correspond to amino acids 661-680, 676-696, 526-545, 874-893, 811-830, 871-891, 856-875, 826-845, 795-815, 736-755, 706-725, 706-725, 691-710, 601-620, 571-590, 556-575, 616-635, 646-665, 631-650, 541-560 and 586-605, respectively, of SEQ ID NO: 161.

[0715] CD4 T cell lines that demonstrated specificity for individual L762P-derived peptides were further expanded by stimulation with the relevant peptide at 10 micrograms/ml. Two weeks post-stimulation, T cell lines were tested using both proliferation and IFN-gamma ELISA assays for recognition of the specific peptide. A number of previously identified T cells continued to demonstrate L762P-peptide specific activity. Each of these lines was further expanded on the relevant peptide and, following two weeks of expansion, tested for specific recognition of the L762P-peptide in titration experiments, as well as for recognition of recombinant E. coli-derived L762P protein. For these experiments, autologous adherent monocytes were pulsed with either the relevant L762P-derived peptide, an irrelevant mammaglobin-derived peptide, recombinant E. coli-derived L762P (approx. 50% pure), or an irrelevant E. coli-derived protein. The majority of T cell lines were found to show low affinity for the relevant peptide, since specific proliferation and IFN-gamma ratios dramatically decreased as L762P peptide was diluted. However, four lines were identified that demonstrated significant activity even at 0.1 micrograms/ml peptide. Each of these lines (referred to as A/D5, D/F5, E/A7 and E/B6) also appeared to specifically proliferate in response to the E. coli-derived L762P protein preparation, but not in response to the irrelevant protein preparation. The amino acid sequences of the L762P-derived peptides recognized by these lines are provided in SEQ ID NO: 234, 249, 236 and 245, respectively. No protein specific IFN-gamma was detected for any of the lines. Lines A/D5, E/A7 and E/B6 were cloned on autologous adherent monocytes pulsed with the relevant peptide at 0.1 (A/D5 and E/A7) or 1 (D/F5) microgram/ml. Following growth, clones were tested for specificity for the relevant peptide. Numerous clones specific for the relevant peptide were identified for lines A/D5 and E/A7.

Example 9 Protein Expression of Lung Tumor-Specific Antigens

[0716] a) Expression of L514S in E. coli

[0717] The lung tumor antigen L514S (SEQ ID NO: 89) was subcloned into the expression vector pE32b at NcoI and NotI sites, and transformed into E. coli using standard techniques. The protein was expressed from residues 3-153 of SEQ ID NO: 89. The expressed amino acid sequence and the corresponding DNA sequence are provided in SEQ ID NO: 252 and 253, respectively.

[0718] b) Expression of L762P

[0719] Amino acids 32-944 of the lung tumor antigen L762P (SEQ ID NO: 161), with a 6× His Tag, were subcloned into a modified pET28 expression vector, using kanamycin resistance, and transformed into BL21 CodonPlus using standard techniques. Low to moderate levels of expression were observed. The determined DNA sequence of the L762P expression construct is provided in SEQ ID NO: 254.

Example 10 Identification of MHC Class II Restricting Allele for L762P Peptide-Specific Responses

[0720] A panel of HLA mismatched antigen presenting cells (APC) were used to identify the MHC class II restricting allele for the L762P-peptide specific responses of CD4 T cell clones derived from lines that recognized L762P peptide and recombinant protein. Clones from two lines, AD-5 and EA-7, were tested as described below. The AD-5 derived clones were found to be restricted by the HLA-DRB-1101 allele, and an EA-7 derived clone was found to be restricted by the HLA DRB-0701 or DQB1-0202 allele. Identification of the restriction allele allows targeting of vaccine therapies using the defined peptide to individuals that express the relevant class II allele. Knowing the relevant restricting allele will also enable clinical monitoring for responses to the defined peptide since only individuals that express the relevant allele will be monitored.

[0721] CD4 T cell clones derived from line AD-5 and EA-7 were stimulated on autologous APC pulsed with the specific peptide at 10 μg/ml, and tested for recognition of autologous APC (from donor D72) as well as against a panel of APC partially matched with D72 at class II alleles. Table 2 shows the HLA class typing of the APC tested. Adherent monocytes (generated by 2 hour adherence) from four different donors, referred to as D45, D187, D208, and D326, were used as APC in these experiments. Autologous APC were not included in the experiment. Each of the APC were pulsed with the relevant peptide (5a for AD-5 and 3e for 3A-7) or the irrelevant mammoglobin peptide at 10 μg/ml, and cultures were established for 10,000 T cells and about 20,000 APC/well. As shown in Table 3, specific proliferation and cytokine production could be detected only when partially matched donor cells were used as APC. Based on the MHC typing analysis, these results strongly suggest that the restricting allele for the L762-specific response of the AD-5 derived clones is HLA-DRB-1101 and for the EA-7 derived clone the restricting allele is HLA DRB-0701 or DQB1-0202. TABLE 2 HLA Typing of APC DONOR DR DR DQ DQ D72 B1-1101 B1-0701 B1-0202 B1-0301 D45 −3 −15 B1-0201 B1-0602 D187 −4 −15 −1 −7 D208 B1-1101 B1-0407 −3 −3 D326 B1-0301 B1-0701 B1-0202 B1-0201

[0722] TABLE 3 L762P Peptide Responses Map to HLA DR Alleles AD-5 A11 B10 C10 C11 E6 F1 γ- γ- γ- γ- γ- γ- Donor Prol IFN Prol IFN Prol IFN Prol IFN Prol IFN Prol IFN D72 46 31 34 24 31 40 DR-0701, -1101, DQ-0202, -7 D45 3.2 1.7 5.5 1.2 3.3 1 1.0 1.5 1.1 1.1 1.6 1.1 DR-3,-15, DQ-1, -0201 D187 1.4 1.2 1.3 1 1.4 1.1 1.4 1.7 1.0 1.1 1.4 1.2 DR-4, -15, DQ-1,-7 D208 138 13 38 5.4 18.8 10 14.6 4.6 15.3 6.1 45.9 8.6 DR-4, -1101, DQ-3 D326 0.7 4 0.3 1 0.3 1.4 1.0 2 0.8 1.1 0.3 1.1 DR-3, -0701, DQ-0202 AD-5 EA-7 F9 G8 G9 G10 G12 γ- γ- γ- γ- γ- Donor Prol IFN Prol IFN Prol IFN Prol IFN Prol IFN D72 55 45 43 91 10 DR-0701, -1101, DQ-0202, -7 D45 1.4 1.3 0.2 1.1 1.1 1.1 1.2 1.5 0.8 1.1 DR-3,-15, DQ-1, -0201 D187 1.2 1.1 0.9 1 1.0 1 1.0 1.6 0.5 1 DR-4, -15, DQ-1,-7 D208 73.3 14.1 38.0 7.7 174.3 16.1 113.6 19.6 0.8 1 DR-4, -1101, DQ-3 D326 0.7 1.1 0.6 1.2 0.4 1 1.2 5 14.1 6.8 DR-3, -0701, DQ-0202

Example 11 Fusion Proteins of N-Terminal and C-Terminal Portions of L763P

[0723] In another embodiment, a Mycobacterium tuberculosis-derived polynucleotide, referred to as Ra12, is linked to at least an immunogenic portion of a polynucleotide of this invention. Ra12 compositions and methods for their use in enhancing expression of heterologous polynucleotide sequences are described in U.S. patent application Ser. No. 60/158,585, the disclosure of which is incorporated herein by reference in its entirety. Briefly, Ra12 refers to a polynucleotide region that is a subsequence of a Mycobacterium tuberculosis MTB32A nucleic acid. MTB32A is a serine protease of 32 KD molecular weight encoded by a gene in virulent and avirulent strains of M. tuberculosis. The nucleotide sequence and amino acid sequence of MTB32A have been described (for example, U.S. patent application Ser. No. 60/158,585; see also, Skeiky et al., Infection and Immun. (1999) 67:3998-4007, incorporated herein by reference). Surprisingly, it was discovered that a 14 KD C-terminal fragment of the MTB32A coding sequence expresses at high levels on its own and remains as a soluble protein throughout the purification process. Moreover, this fragment may enhance the immunogenicity of heterologous antigenic polypeptides with which it is fused. This 14 KD C-terminal fragment of the MTB32A is referred to herein as Ra12 and represents a fragment comprising some or all of amino acid residues 192 to 323 of MTB32A.

[0724] Recombinant nucleic acids which encode a fusion polypeptide comprising a Ra12 polypeptide and a heterologous lung tumor polypeptide of interest, can be readily constructed by conventional genetic engineering techniques. Recombinant nucleic acids are constructed so that, preferably, a Ra12 polynucleotide sequence is located 5′ to a selected heterologous lung tumor polynucleotide sequence. It may also be appropriate to place a Ra12 polynucleotide sequence 3′ to a selected heterologous polynucleotide sequence or to insert a heterologous polynucleotide sequence into a site within a Ra12 polynucleotide sequence.

[0725] In addition, any suitable polynucleotide that encodes a Ra12 or a portion or other variant thereof can be used in constructing recombinant fusion polynucleotides comprising Ra12 and one or more lung tumor polynucleotides disclosed herein. Preferred Ra12 polynucleotides generally comprise at least about 15 consecutive nucleotides, at least about 30 nucleotides, at least about 60 nucleotides, at least about 100 nucleotides, at least about 200 nucleotides, or at least about 300 nucleotides that encode a portion of a Ra12 polypeptide.

[0726] Ra12 polynucleotides may comprise a native sequence (i.e., an endogenous sequence that encodes a Ra12 polypeptide or a portion thereof) or may comprise a variant of such a sequence. Ra12 polynucleotide variants may contain one or more substitutions, additions, deletions and/or insertions such that the biological activity of the encoded fusion polypeptide is not substantially diminished, relative to a fusion polypeptide comprising a native Ra12 polypeptide. Variants preferably exhibit at least about 70% identity, more preferably at least about 80% identity and most preferably at least about 90% identity to a polynucleotide sequence that encodes a native Ra12 polypeptide or a portion thereof.

[0727] Two specific embodiments of fusions between Ra12 and antigens of the present invention are described in this example.

[0728] A. N-Terminal Portion of L763P

[0729] A fusion protein of full-length Ra12 and the N-terminal portion of L763P (referred to as L763P-N; amino acid residues 1-130 of SEQ ID NO: 159) was expressed as a single recombinant protein in E. coli. The cDNA for the N-terminal portion was obtained by PCR with a cDNA for the full length L763P and primers L763F3 (5′ CGGCGAATTCATGGATTGGGGGACGCTGC; SEQ ID NO: 383) and 1763RV3 (5′ CGGCCTCGAGTCACCCCTCTATCCGAACCTTCTGC; SEQ ID NO: 384). The PCR product with expected size was recovered from agarose gel, digested with restriction enzymes EcoRI and Xhol, and cloned into the corresponding sites in the expression vector pCRX1. The sequence for the fusion of full-length of Ra12 and L763P-N was confirmed by DNA sequencing. The determined cDNA sequence is provided in SEQ ID NO: 351, with the corresponding amino acid sequence being provided in SEQ ID NO: 352).

[0730] B. C-Terminal Portion of L763P

[0731] A fusion protein of full-length Ra12 and the C-terminal portion of L763P (referred to as L763P-C; amino acid residues 100-262 of SEQ ID NO: 159) was expressed as a single recombinant protein in E. coli. The EDNA of the C-terminal portion of L763P was obtained by PCR with a cDNA for the full length of L763P and primers L763F4 (5′ CGGCGAATTCCACGAACCACTCGCAAGTTCAG; SEQ ID NO: 385) and L763RV4 (5′ CGGCTCGAG-TTAGCTTGGGCCTGTGATTGC; SEQ ID NO: 386). The PCR product with expected size was recovered from agarose gel, digested with restriction enzymes EcoRI and XhoI, and cloned into the corresponding sites in the expression vector pCRX1. The sequence for the fusion of full-length Ra12 and L763P-C was confirmed by DNA sequencing. The determined DNA sequence is provided in SEQ ID NO: 353, with the corresponding amino acid sequence being provided in SEQ ID NO: 354.

[0732] The recombinant proteins described in this example are useful for the preparation of vaccines, for antibody therapeutics, and for diagnosis of lung tumors.

Example 12 Expression of E. coli of L762P His Tag Fusion Protein

[0733] PCR was performed on the L762P coding region with the following primers:

[0734] Forward primer starting at amino acid 32.

[0735] PDM-278 5′ggagtacagcttcaagacaatggg 3′ (SEQ ID NO: 355) Tm 57° C.

[0736] Reverse primer including natural stop codon after amino acid 920, creating EcoRI site

[0737] PDM-280 5′ccatgggaattcattataataattttgttcc 3′ (SEQ ID NO: 356) TM55° C.

[0738] The PCR product was digested with EcoRI restriction enzyme, gel purified and then cloned into pPDM His, a modified pET28 vector with a His tag in frame, which had been digested with Eco72I and EcoRI restriction enzymes. The correct construct was confirmed by DNA sequence analysis and then transformed into BL21 (DE3) pLys S and BL21 (DE3) CodonPlus RIL expression hosts.

[0739] The protein sequence of expressed recombinant L762P is shown in SEQ ID NO: 357, and the DNA sequence is shown in SEQ ID NO: 358.

Example 13 Expression in E. coli of a L773P His Tag Fusion Protein

[0740] The L773PA coding region (encoding amino acids 2-71 of SEQ ID NO: 172) was PCR amplified using the following primers:

[0741] Forward primer for L773PA starting at amino acid 2:

[0742] PDM-299 5′tggcagcccctcttcftcaagtggc 3′ (SEQ ID NO: 359) Tm63° C.

[0743] Reverse primer for L773PA creating artificial stop codon after amino acid 70:

[0744] PDM-355 5′cgccagaattcatcaaacaaatctgttagcacc 3′ (SEQ ID NO: 360) Tm62° C.

[0745] The resulting PCR product was digested with EcoRI restriction enzyme, gel purified and then cloned into pPDM His, a modified pET28 vector with a His tag in frame, which had been digested with Eco72I and EcoRI restriction enzymes. The correct construct was confirmed by DNA sequence analysis and transformed into BL21 (DE3) pLys S and BL21 (DE3) CodonPlus RIL expression hosts.

[0746] The protein sequence of expressed recombinant L773PA is shown in SEQ ID NO: 361, and the DNA sequence is shown in SEQ ID NO: 362.

Example 14 Identification of Epitopes Derived from Lung Tumor Specific Polypeptides

[0747] A series of peptides from the L773P amino acid sequence (SEQ ID NO: 172) were synthesized and used in in vitro priming experiments to generate peptide-specific CD4 T cells. These peptides were 20-mers that overlapped by 15 amino acids and corresponded to amino acids 1-69 of the L773P protein. This region has been demonstrated to be tumor-specific. Following three in vitro stimulations, CD4 T cell lines were identified that produced IFNγ in response to the stimulating peptide but not the control peptide. Some of these T cell lines demonstrated recognition of recombinant L773P and L773PA (tumor-specific region) proteins.

[0748] To perform the experiments, a total of eleven 20-mer peptides overlapping by 15 amino acids and derived from the N-terminal tumor-specific region of L773P (corresponding to amino acids 1-69 of SEQ ID NO: 172) were generated by standard procedures (FIG. 1; SEQ ID NO: 363, 387, 388, 365 and 389-395, respectively). Dendritic cells were derived from PBMC of a normal donor using GMCSF and IL-4 by standard protocol. Purified CD4 T cells were generated from the same donor as the dendritic cells using MACS beads and negative selection of PBMCs. Dendritic cells were pulsed overnight with the individual 20-mer peptides at a concentration of 10 μg/ml. Pulsed dendritic cells were washed and plated at 1×10⁴/well of a 96-well U-bottom plates, and purified CD4 cells were added at 1×10⁵ well. Cultures were supplemented with 10 ng/ml IL-6 and 5 ng/ml IL-12, and incubated at 37° C. Cultures were re-stimulated as above on a weekly basis using as APC dendritic cells generated and pulsed as above, supplemented with 5 ng/ml IL-7 and 10 μg/ml IL-2. Following 3 in vitro stimulation cycles, cell lines (each corresponding to one well) were tested for cytokine production in response to the stimulating peptide vs. an irrelevant peptide.

[0749] A small number of individual CD4 T cell lines (9/528) demonstrated cytokine release (IFNγ) in response to the stimulating peptide but not to control peptide (FIG. 3). The CD4 T cell lines that demonstrated specific activity were restimulated on the appropriate L773P peptide and reassayed using autologous dendritic cells pulsed with 10 μg/ml of the appropriate L773P peptide, an irrelevant control peptide, recombinant L773P protein (amino acids 2-364, made in E. coli), recombinant L773PA (amino acids 2-71, made in E. coli), or an appropriate control protein (L3E, made in E. coli). Three of the nine lines tested (1-3C, 1-6G, and 4-12B) recognized the appropriate L773P peptide as well as recombinant L773P and L773PA (FIG. 2). Four of the lines tested (4-8A, 4-8E, 4-12D, and 4-12E) recognized the appropriate L773P peptide only. Two of the lines tested (5-6F and 9-3B) demonstrated non-specific activity.

[0750] These results demonstrate that the peptide sequences MWQPLFFKWLLSCCPGSSQI (amino acids 1-20 of SEQ ID NO: 172; SEQ ID NO: 363) and GSSQIAAAASTQPEDDINTQ (amino acids 16-35 of SEQ ID NO: 172; SEQ ID NO: 365) may represent naturally processed epitopes of L773P, which are capable of stimulating human class II MHC-restricted CD4 T cell responses.

[0751] In subsequent studies, the above epitope mapping experiment was repeated using a different donor. Again, some of the resulting T cell lines were found to respond to peptide and recombinant protein. An additional peptide was found to be naturally processed. Specifically, purified CD4 cells were stimulated on a total of eleven 20-mer peptides overlapping by 15 amino acids (SEQ ID NO: 363, 387, 388, 365 and 389-395, respectively). The priming was carried out as described above, except that a peptide concentration of 0.5 ug/mL rather than 10 ug/mL was employed. In the initial screen of the cell lines 9 of the 528 lines released at least a three-fold greater level of IFN-gamma with stimulating peptide vs. control peptide. These 9 lines were restimulated on the appropriate peptide and then tested on dendritic cells pulsed with a titration of appropriate peptide (10 ug/mL, 1 ug/mL and 0.1 ug/mL), and 10 ug/mL of a control peptide. Six of the 9 lines recognized recombinant L773P as well as peptide. The six lines referred to as 1-1E, 1-2E, 1-4H, 1-6A, 1-6G and 2-12B recognized L773PA and the appropriate peptide. These results demonstrate that the peptides of SEQ ID NO: 363 and 387 represent naturally processed epitopes of L773P.

[0752] Using the procedures described above, CD4+T cell responses were generated from PBMC of normal donors using dendritic cells pulsed with overlapping 20-mer peptides (SEQ ID NO: 396-419) spanning the L523S polypeptide sequence (SEQ ID NO: 176). A number of CD4+ T cells demonstrated reactivity with the priming peptides as well as with L523S recombinant protein, with the dominant reactivity of these lines being within the peptides 4, 7 and 21 (SEQ ID NO: 399, 402 and 416; corresponding to amino acids 30-39, 60-79 and 200-219, respectively, of SEQ ID NO: 176).

[0753] Epitopes within the scope of the invention include epitopes restricted by other class II MHC molecules. In addition, variants of the peptide can be produced wherein one or more amino acids are altered such that there is no effect on the ability of the peptides to bind to MHC molecules, no effect on their ability to elicit T cell responses, and no effect on the ability of the elicited T cells to recognize recombinant protein.

Example 15 Surface Expression of L762P and Antibody Epitopes Thereof

[0754] Rabbits were immunized with full-length histidine-tagged L762P protein generated in E. coli. Sera was isolated from rabbits and screened for specific recognition of L762P in ELISA assays. One polyclonal serum, referred to as 2692L, was identified that specifically recognized recombinant L762P protein. The 2692L anti-L762P polyclonal antibodies were purified from the serum by affinity purification using L762P affinity columns. Although L762P is expressed in a subset of primary lung tumor samples, expression appears to be lost in established lung tumor cell lines. Therefore, to characterize surface expression of L762P, a retrovirus construct that expresses L762P was used to transduce primary human fibroblasts as well as 3 lung tumor cell lines (522-23, HTB, and 343T). Transduced lines were selected and expanded to examine L762P surface expression by FACS analysis. For this analysis, non-transduced and transduced cells were harvested using cell dissociation medium, and incubated with 10-50 micrograms/ml of either affinity purified anti-L762P or irrelevant antisera. Following a 30 minute incubation on ice, cells were washed and incubated with a secondary, FITC conjugated, anti rabbit IgG antibody as above. Cells were washed, resuspended in buffer with Propidium Iodide (PI) and examined by FACS using an Excalibur fluorescence activated cell sorter. For FACS analysis, PI-positive (i.e., dead/permeabilized cells) were excluded. The polyclonal anti-L762P sera specifically recognized and bound to the surface of L762P-transduced cells but not the non-transduced counterparts. These results demonstrate that L762P is localized to the cell surface of both fibroblasts as well as lung tumor cells.

[0755] To identify the peptide epitopes recognized by 2692L, an epitope mapping approach was pursued. A series of overlapping 19-21 mers (5 amino acid overlap) was synthesized that spanned the C terminal portion of L762P (amino acids 481-894 of SEQ ID NO: 161). In an initial experiment peptides were tested in pools. Specific reactivity with the L762P antiserum was observed with pools A, B, C, and E. To identify the specific peptides recognized by the antiserum, flat bottom 96 well microtiter plates were coated with individual peptides at 10 microgram/ml for 2 hours at 37° C. Wells were then aspirated and blocked with phosphate buffered saline containing 5% (w/v) milk for 2 hours at 37° C., and subsequently washed in PBS containing 0.1% Tween 20 (PBST). Purified rabbit anti-L762P serum 2692L was added at 200 or 20 ng/well to triplicate wells in PBST and incubated overnight at room temperature. This was followed by washing 6 times with PBST and subsequently incubating with HRP-conjugated donkey anti rabbit IgG (H+L)Affinipure F(ab′) fragment at 1:2,000 for 60 minutes. Plates were then washed, and incubated in tetramethyl benzidine substrate. Reactions were stopped by the addition of 1N sulfuric acid and plates were read at 450/570 nm using an ELISA plate reader.

[0756] The resulting data, presented in Table 4 below, demonstrates that the L762P antisera recognized at least 6 distinct peptide epitopes from the 3′ half of L762P. TABLE 4 Elisa activity (OD 450-570) Peptide (starting 200 ng 20 ng amino acid of L762P) pool polyclonal serum polyclonal serum A (481) A 1.76 1.0 B (405) A 0.14 .06 C (511) E 0.47 0.18 D (526) E 0.11 0.09 E (541) A 0.11 0.04 F (556) A 0.04 0.02 G (571) A 0.06 0.02 H (586) B 0.1 0.03 I (601) B 0.25 0.06 J (616) B 0.1 0.03 K (631) E 0.1 0.08 L (646) B 0.28 0.12 M (661) B 0.14 0.03 N (676) C 0.12 0.1 O (691) C 1.1 0.23 P (706) C 0.1 0.03 Q (721) C 0.11 0.05 R (736) E 0.12 0.04 S (751) C 0.15 0.06 U (781) D 0.12 0.06 V (795) F 0.07 0.05 X (826) D 0.1 0.03 Y (841) D 0.17 0.07 Z (856) D 0.16 0.08 AA (871) F 0.17 0.05 BB (874) F 0.14 0.11 No Peptide 0.15 0.045

[0757] Individual peptides were identified from each of the pools, and additionally a weak reactivity was identified with peptide BB from pool F. The relevant peptide epitopes are summarized in the Table 5 below. The amino acid sequences for peptides BB, O, L, I, A and C are provided in SEQ ID NO: 376-381, respectively, with the corresponding cDNA sequences being provided in SEQ ID NO: 373, 370, 372, 374, 371 and 375, respectively. TABLE 5 Amino ELISA activity Nucleotides acids of (OD 450-570) Peptide of L762P L762P Sequence pool 200 ng 20 ng A 1441-1500 481-500 SRISSGTGDTFQQHIQLEST A 1.76 1.0 C 1531-1590 511-530 KNTVTVDNTVGNDTMFLVTW E 0.47 0.18 I 1801-1860 601-620 AVPPATVEAFVERDSLHFPH B 0.25 0.06 L 1936-1955 646-665 PETGDPVTLRLLDDGAGADV B 0.28 0.12 O 2071-2130 691-710 VNHSPSISTPAHSIPGSHAMIL C 1.1 0.23 BB 2620-2679 874-893 LQSAVSNIAQAPLFIPPNSD F 0.14 0.11 None — —     — — 0.15 0.05

Example 16 Detection of Antibodies Against Lung Tumor Antigens in Patient Sera

[0758] Antibodies specific for the lung tumor antigens L773P (SEQ ID NO: 172), L514S (SEQ ID NO: 155 and 156), L523S (SEQ ID NO: 176), L762P (SEQ ID NO: 161) and L763P (SEQ ID NO: 159) were shown to be present in effusion fluid or sera of lung cancer patients but not in normal donors. More specifically, the presence of antibodies against L773P, L514S, L523S, L762P and L763P in effusion fluid obtained from lung cancer patients and in sera from normal donors was detected by ELISA using recombinant proteins and HRP-conjugated anti-human Ig. Briefly, each protein (100 ng) was coated in 96-well plate at pH 9.5. In parallel, BSA (bovine serum albumin) was also coated as a control protein. The signals ([S], absorbance measured at 405 nm) against BSA ([N]) were determined. The results of these studies are shown in Table 6, wherein—represents [S]/[N]<2; +/− represents [S]/[N]>2; ++ represents [S]/[N]>3; and +++ represents [S]/[N] >5. TABLE 6 Detection of Antibodies against Lung Tumor Antigens L514S L523S L762P L763P L773PA Effusion fluid #1  +++ ++ ++ − ++ #2  − − +/− ++ +/− #3  − − − − +/− #4  +/− ++ +/− − +/− #5  +/− +++ +/− +/− ++ #7  − +/− − − +/− #8  − +++ − − ++ #10 − ++ +/− +/− − #11 +/− ++ ++ − ++ #12 +++ +/− − +/− +/− #13 − +/− − − +/− #14 − +++ +/− +/− ++ #15 +/− ++ +/− − ++ #17 − +/− − − +/− #18 − ++ − − − #19 − +/− − − +/− #20 +/− +/− +/− − +/− Normal sera #21 − +/− − − − #22 − − − − − #23 − − − − +/− #24 − +/− − − − #25 +/− +/− − − +/−

[0759] Using Western blot analyses, antibodies against L523S were found to be present in 3 out of 4 samples of effusion fluid from lung cancer patients, with no L523S antibodies being detected in the three samples of normal sera tested.

Example 17 Expression in E. coli of a L514S His Tag Fusion Protein

[0760] PCR was performed on the L514S-13160 coding region with the following primers:

[0761] Forward primer PDM-278 5′ cacactagtgtccgcgtggcggcctac 3′ (SEQ ID NO: 421) Tm 67° C.

[0762] Reverse primer PDM-280 5′ catgagaattcatcacatgcccttgaaggctccc 3′ (SEQ ID NO: 422) TM 66° C.

[0763] The PCR conditions were as follows:

[0764] 10 μl 10× Pfu buffer

[0765] 1.0 μl 10 mM dNTPs

[0766] 2.0 μl 10 μM each primer

[0767] 83 μl sterile water

[0768] 1.5 μl Pfu DNA polymerase (Stratagene, La Jolla, Calif.)

[0769] 50 ηg DNA

[0770] 96° C. for 2 minutes, 96° C. for 20 seconds, 66° C. for 15 seconds, 72° C. for 1 minute with 40 cycles and then 72° C. for 4 minutes.

[0771] The PCR product was digested with EcoRI restriction enzyme, gel purified and then cloned into pPDM His, a modified pET28 vector with a His tag in frame, which had been digested with Eco72I and EcoRI restriction enzymes. The correct construct was confirmed by DNA sequence analysis and then transformed into BL21 CodonPlus (Stratagene, La Jolla, Calif.) cells for expression.

[0772] The amino acid sequence of expressed recombinant L514S is shown in SEQ ID NO: 423, and the DNA coding region sequence is shown in SEQ ID NO: 424.

Example 18 Expression in E. coli of a L523S His Tag Fusion Protein

[0773] PCR was performed on the L523S coding region with the following primers:

[0774] Forward primer PDM-414 5′ aacaaactgtatatcggaaacctcagcgagaa 3′ (SEQ ID NO: 425) Tm 62° C.

[0775] Reverse primer PDM-415 5′ ccatagaattcattacttccgtcttgactgagg 3′ (SEQ ID NO: 426) TM 62° C.

[0776] The PCR conditions were as follows:

[0777] 10 μl 10× Pfu buffer

[0778] 1.0 μl 10 mM dNTPs

[0779] 2.0 μl 10 μM each primer

[0780] 83 μl sterile water

[0781] 1.5 μl Pfu DNA polymerase (Stratagene, La Jolla, Calif.)

[0782] 50 ηg DNA

[0783] 96° C. for 2 minutes, 96° C. for 20 seconds, 62° C. for 15 seconds, 72° C. for 4 minutes with 40 cycles and then 72° C. for 4 minutes.

[0784] The PCR product was digested with EcoRI restriction enzyme, gel purified and then cloned into pPDM His, a modified pET28 vector with a His tag in frame, which had been digested with Eco72I and EcoRI restriction enzymes. The correct construct was confirmed by DNA sequence analysis and then transformed into BL21 CodonPlus (Stratagene, La Jolla, Calif.) cells for expression.

[0785] The amino acid sequence of expressed recombinant L523S is shown in SEQ ID NO: 427, and the DNA coding region sequence is shown in SEQ ID NO: 428.

Example 19 Expression in E. coli of a L762PA His Tag Fusion Protein

[0786] PCR was performed on the L762PA coding region (L762PA is missing the signal sequence, the C-terminal transmembrane domain and the cytoplasmic tail) with the following primers:

[0787] Forward primer PDM-278 5′ggagtacagcttcaagacaatggg 3′ (SEQ ID NO: 355) Tm 57° C.

[0788] Reverse primer PDM-279 5′ccatggaattcattatttcaatataagataatctc 3′ (SEQ ID NO: 429) TM56° C.

[0789] The PCR conditions were as follows:

[0790] 10 μl 10× Pfu buffer

[0791] 1.0 μl 10 mM dNTPs

[0792] 2.0 μl 10 μM each primer

[0793] 83 μl sterile water

[0794] 1.5 μl Pfu DNA polymerase (Stratagene, La Jolla, Calif.)

[0795] 50 ηg DNA

[0796] 96° C. for 2 minutes, 96° C. for 20 seconds, 55° C. for 15 seconds, 72° C. for 5 minutes with 40 cycles and then 72° C. for 4 minutes.

[0797] The PCR product was digested with EcoRI restriction enzyme, gel purified and then cloned into pPDM His, a modified pET28 vector with a His tag in frame, which had been digested with Eco72I and EcoRI restriction enzymes. The correct construct was confirmed by DNA sequence analysis and then transformed into BL21 pLys S (Novagen, Madison, Wis.) cells for expression.

[0798] The amino acid sequence of expressed recombinant L762PA is shown in SEQ ID NO: 430, and the DNA coding region sequence is shown in SEQ ID NO: 431.

Example 20 Expression in E. coli of a L773P His Tag Fusion Protein

[0799] PCR was performed on the L773P coding region with the following primers:

[0800] Forward primer PDM-299 5′ tggcagcccctcttcttcaagtggc 3′ (SEQ ID NO: 359) Tm 63° C.

[0801] Reverse primer PDM-300 5′ cgcctgctcgagtcattaatattcatcagaaaatgg 3′ (SEQ ID NO: 432) TM 63° C.

[0802] The PCR conditions were as follows:

[0803] 10 μl 10× Pfu buffer

[0804] 1.0 μl 10 mM dNTPs

[0805] 2.0 μl 10 μM each primer

[0806] 83 μl sterile water

[0807] 1.5 μl Pfu DNA polymerase (Stratagene, La Jolla, Calif.)

[0808] 50 ηg DNA

[0809] 96° C. for 2 minutes, 96° C. for 20 seconds, 63° C. for 15 seconds, 72° C. for 2 minutes 15 seconds with 40 cycles and then 72° C. for 4 minutes.

[0810] The PCR product was digested with EcoRI restriction enzyme, gel purified and then cloned into pPDM His, a modified pET28 vector with a His tag in frame, which had been digested with Eco72I and EcoRI restriction enzymes. The correct construct was confirmed by DNA sequence analysis and then transformed into BL21 pLys S (Novagen, Madison, Wis.) and BL21 CodonPlus (Stratagene, La Jolla, Calif.) cells for expression.

[0811] The amino acid sequence of expressed recombinant L773P is shown in SEQ ID NO: 433, and the DNA coding region sequence is shown in SEQ ID NO: 434.

Example 21 Cloning and Sequencing of a T Cell Receptor Clone for the Lung Specific Antigen L762P

[0812] T cell receptor (TCR) alpha and beta chains from a CD4 T cell clone specific for the lung specific antigen L762P were cloned and sequence. Basically, total mRNA from 2×10⁶ cells from CTL clone 4H6 was isolated using Trizol reagent and cDNA was synthesized using Ready-to go kits (Pharmacia). To determine Valpha and Vbeta sequences of this clone, a panel of Valpha and Vbeta subtype specific primers was synthesized and used in RT-PCR reactions with cDNA generated from each of the clones. The RT-PCR reactions demonstrated that each of the clones expressed a common Vbeta sequence that corresponded to the Vbeta8 subfamily and a Valpha sequence that corresponded to the Valpha8 subfamily. To clone the full TCR alpha and beta chains from clone 4H6, primers were designed that spanned the initiator and terminator-coding TCR nucleotides. The primers were as follows:

[0813] forward primer for TCR Valpha8 5′ ggatccgccgccaccatgacatccattcgagctgta 3′ (SEQ ID NO: 435; has a BamHI site inserted);

[0814] Kozak reverse primer for TCR Valpha8 (antisense) 5′ gtcgactcagctggaccacagccgcag 3′ (SEQ ID NO: 436; has a SalI site inserted plus the TCR alpha constant sequence);

[0815] forward primer for TCR Vbeta8 (sense) 5′ ggatccgccgccaccatggactcctggaccttctgct 3′ (SEQ ID NO: 437; has a BamHI site inserted); and

[0816] Kozak reverse primer for TCR Vbeta 5′ gtcgactcagaaatcctttctcttgac 3′ (SEQ ID NO: 438; has a SalI site inserted plus the TCR beta constant sequence).

[0817] Standard 35 cycle RT-PCR reactions were established using the cDNA synthesized from the CTL clone and the above primers utilizing the proofreading thermostable polymerase, PWO (Roche). The resultant PCR band, about 850 bp for Valpha and about 950 for Vbeta, was ligated into a PCR blunt vector (Invitrogen) and transformed into E. coli. E. coli transformed with plasmids having full-length alpha and beta chains were identified. Large scale preparations of the corresponding plasmids were generated, and these plasmids were sequenced. The Valpha sequence (SEQ ID NO: 439) was shown by nucleotide sequence alignment to be homologous to Valpha8.1, while the Vbeta sequence (SEQ ID NO: 440) was shown by nucleotide sequence alignment to be homologous to Vbeta8.2.

Example 22 Recombinant Expression of Full Length L762P in Mammalain Cells

[0818] Full length L762P cDNA was subcloned into the mammalian expression vectors VR1012 and pCEP4 (Invitrogen). Both expression vectors had previously been modified to contain a FLAG epitope tag. These constructs were transfected into HEK293 and CHL-1 cells (ATCC) using Lipofectamine 2000 reagent (Gibco). Briefly, both the HEK and CHL-1 cells were plated at a density of 100,000 cells/ml in DMEM (Gibco) containing 10% FBS (Hyclone) and grown overnight. The following day, 4 μl of Lipofectamine 2000 was added to 100 μl of DMEM containing no FBS and incubated for 5 minutes at room temperature. The Lipofectamine/DMEM mixture was then added to 1 μg of L762P Flag/pCEP4 or L762P Flag/VR1012 plasmid DNA resuspended in 100 μl DMEM and incubated for 15 minutes at room temperature. The Lipofectamine/DNA mix was then added to the HEK293 and CHL-1 cells and incubated for 48-72 hours at 37° C. with 7% CO₂. Cells were rinsed with PBS, then collected and pelleted by centrifugation. L672P expression was detected in the transfected HEK293 and CHL-1 cell lysates by Western blot analysis and was detected on the surface of transfected HEK cells by flow cytometry analysis.

[0819] For Western blot analysis, whole cell lysates were generated by incubating the cells in Triton-X100 containing lysis buffer for 30 minutes on ice. Lysates were then cleared by centrifugation at 10,000 rpm for 5 minutes at 4° C. Samples were diluted with SDS-PAGE loading buffer containing beta-mercaptoethanol, then boiled for 10 minutes prior to loading the SDS-PAGE gel. The protein was transferred to nitrocellulose and probed using 1 ug/ml purified anti-L762P rabbit polyclonal sera (lot #690/73) or non-diluted anti-L762P mAb 153.20.1 supernatant. Blots were revealed using either goat anti-rabbit Ig coupled to HRP or goat anti-mouse Ig coupled to HRP followed by incubation in ECL substrate.

[0820] For flow cytometric analysis, cells were washed further with ice cold staining buffer (PBS+1%BSA +Azide). Next, the cells were incubated for 30 minutes on ice with 10 ug/ml of purified anti-L762P polyclonal sera (lot #690/73) or a 1:2 dilution of anti-L762P mAb 153.20.1 supernatant. The cells were washed 3 times with staining buffer and then incubated with a 1:100 dilution of goat anti-rabbit Ig(H+L)-FITC or goat anti-mouse Ig(H+L)-FITC reagent (Southern Biotechnology) for 30 minutes on ice. After 3 washes, the cells were resuspended in staining buffer containing propidium iodide (PI), a vital stain that allows for the exclusion of permeable cells, and analyzed by flow cytometry.

[0821] From the foregoing it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.

1 440 1 315 DNA Homo sapien misc_feature (1)...(315) n = A,T,C or G 1 gcagagacag actggtggtt gaacctggag gtgccaaaaa agccagctgc gggcccagga 60 cagctgccgt gagactcccg atgtcacagg cagtctgtgt ggttacagcg cccctcagtg 120 ttcatctcca gcagagacaa cggaggaggc tcccaccagg acggttctca ttatttatat 180 gttaatatgt ttgtaaactc atgtacagtt ttttttgggg gggaagcaat gggaanggta 240 naaattacaa atagaatcat ttgctgtaat ccttaaatgg caaacggtca ggccacgtga 300 aaaaaaaaaa aaaaa 315 2 380 DNA Homo sapien 2 atttaggctt aagattttgt ttacccttgt tactaaggag caaattagta ttaaagtata 60 atatatataa acaaatacaa aaagttttga gtggttcagc ttttttattt tttttaatgg 120 cataactttt aacaacactg ctctgtaatg ggttgaactg tggtactcag actgagataa 180 ctgaaatgag tggatgtata gtgttattgc ataattatcc cactatgaag caaagggact 240 ggataaattc ccagtctaga ttattagcct ttgttaacca tcaagcacct agaagaagaa 300 ttattggaaa ttttgtcctc tgtaactggc actttggggt gtgacttatc ttttgccttt 360 gtaaaaaaaa aaaaaaaaaa 380 3 346 DNA Homo sapien misc_feature (1)...(346) n = A,T,C or G 3 ttgtaagtat acaattttag aaaggattaa atgttattga tcattttact gaatactgca 60 catcctcacc atacaccatc cactttccaa taacatttaa tcctttctaa aattgtaagt 120 atacaattgt actttctttg gattttcata acaaatatac catagactgt taattttatt 180 gaagtttcct taatggaatg agtcattttt gtcttgtgct tttgaggtta cctttgcttt 240 gacttccaac aatttgatca tatagtgttg agctgtggaa atctttaagt ttattctata 300 gcaataattt ctattnnnag annccnggnn naaaannann annaaa 346 4 372 DNA Homo sapien misc_feature (1)...(372) n = A,T,C or G 4 actagtctca ttactccaga attatgctct tgtacctgtg tggctgggtt tcttagtcgt 60 tggtttggtt tggttttttg aactggtatg tagggtggtt cacagttcta atgtaagcac 120 tctcttctcc aagttgtgct ttgtggggac aatcattctt tgaacattag agaggaaggc 180 agttcaagct gttgaaaaga ctattgctta tttttgtttt taaagaccta cttgacgtca 240 tgtggacagt gcacgtgcct tacgctacat cttgttttct aggaagaagg ggatgcnggg 300 aaggantggg tgctttgtga tggataaaac gnctaaataa cacaccttta cattttgaaa 360 aaaacaaaac aa 372 5 698 DNA Homo sapien misc_feature (1)...(698) n = A,T,C or G 5 actagtanga tagaaacact gtgtcccgag agtaaggaga gaagctacta ttgattagag 60 cctaacccag gttaactgca agaagaggcg ggatactttc agctttccat gtaactgtat 120 gcataaagcc aatgtagtcc agtttctaag atcatgttcc aagctaactg aatcccactt 180 caatacacac tcatgaactc ctgatggaac aataacaggc ccaagcctgt ggtatgatgt 240 gcacacttgc tagactcaga aaaaatacta ctctcataaa tgggtgggag tattttgggt 300 gacaacctac tttgcttggc tgagtgaagg aatgatattc atatnttcat ttattccatg 360 gacatttagt tagtgctttt tatataccag gcatgatgct gagtgacact cttgtgtata 420 tntccaaatn ttngtncngt cgctgcacat atctgaaatc ctatattaag antttcccaa 480 natgangtcc ctggtttttc cacgccactt gatcngtcaa ngatctcacc tctgtntgtc 540 ctaaaaccnt ctnctnnang gttagacngg acctctcttc tcccttcccg aanaatnaag 600 tgtgngaaga nanccncncn cccccctncn tncnncctng ccngctnnnc cncntgtngg 660 gggngccgcc cccgcggggg gacccccccn ttttcccc 698 6 740 DNA Homo sapien misc_feature (1)...(740) n = A,T,C or G 6 actagtcaaa aatgctaaaa taatttggga gaaaatattt tttaagtagt gttatagttt 60 catgtttatc ttttattatg tnttgtgaag ttgtgtcttt tcactaatta cctatactat 120 gccaatattt ccttatatct atccataaca tttatactac atttgtaaga gaatatgcac 180 gtgaaactta acactttata aggtaaaaat gaggtttcca agatttaata atctgatcaa 240 gttcttgtta tttccaaata gaatggactt ggtctgttaa ggggctaagg gagaagaaga 300 agataaggtt aaaagttgtt aatgaccaaa cattctaaaa gaaatgcaaa aaaaaattta 360 ttttcaagcc ttcgaactat ttaaggaaag caaaatcatt tcctanatgc atatcatttg 420 tgagantttc tcantaatat cctgaatcat tcatttcagc tnaggcttca tgttgactcg 480 atatgtcatc tagggaaagt ctatttcatg gtccaaacct gttgccatag ttggtnaggc 540 tttcctttaa ntgtgaanta ttnacangaa attttctctt tnanagttct tnatagggtt 600 aggggtgtgg gaaaagcttc taacaatctg tagtgttncg tgttatctgt ncagaaccan 660 aatnacggat cgnangaagg actgggtcta tttacangaa cgaatnatct ngttnnntgt 720 gtnnncaact ccngggagcc 740 7 670 DNA Homo sapien misc_feature (1)...(670) n = A,T,C or G 7 gctggggagc tcggcatggc ggtccccgct gcagccatgg ggccctcggc gttgggccag 60 agcggccccg gctcgatggc cccgtggtgc tcagtgagca gcggcccgtc gcgctacgtg 120 cttgggatgc aggagctgtt ccggggccac agcaagaccg cgagttcctg gcgcacagcg 180 ccaaggtgca ctcggtggcc tggagttgcg acgggcgtcg cctacctcgg ggtcttcgac 240 aagacgccac gtcttcttgc tgganaanga ccgttggtca aagaaaacaa ttatcgggga 300 catggggata gtgtggacca ctttgttggc atccaagtaa tcctgaccta tttgttacgg 360 cgtctggaga taaaaccatt cgcatctggg atgtgaggac tacaaaatgc attgccactg 420 tgaacactaa aggggagaac attaatatct gctggantcc tgatgggcan accattgctg 480 tagcnacaag gatgatgtgg tgactttatt gatgccaaga aaccccgttc caaagcaaaa 540 aaacanttcc aanttcgaag tcaccnaaat ctcctggaac aatgaacatn aatatnttct 600 tcctgacaat ggnccttggg tgtntcacat cctcagctnc cccaaaactg aancctgtnc 660 natccacccc 670 8 689 DNA Homo sapien misc_feature (1)...(689) n = A,T,C or G 8 actagtatct aggaatgaac agtaaaagag gagcagttgg ctacttgatt acaacagagt 60 aaatgaagta ctggatttgg gaaaacctgg ttttattaga acatatggaa tgaaagccta 120 cacctagcat tgcctactta gccccctgaa ttaacagagc ccaattgaga caaacccctg 180 gcaacaggaa attcaaggga gaaaaagtaa gcaacttggg ctaggatgag ctgactccct 240 tagagcaaag ganagacagc ccccattacc aaataccatt tttgcctggg gcttgtgcag 300 ctggcagtgt tcctgcccca gcatggcacc ttatngtttt gatagcaact tcgttgaatt 360 ttcaccaact tattacttga aattataata tagcctgtcc gtttgctgtn tccaggctgt 420 gatatatntt cctagtggtt tgactttnaa aataaatnag gtttantttt ctccccccnn 480 cnntnctncc nntcnctcnn cnntcccccc cnctcngtcc tccnnnnttn gggggggccn 540 cccccncggn ggacccccct ttggtccctt agtggaggtt natggcccct ggnnttatcc 600 nggccntann tttccccgtn nnaaatgntt ccccctccca ntcccnccac ctcaanccgg 660 aagcctaagt ttntaccctg ggggtcccc 689 9 674 DNA Homo sapien misc_feature (1)...(674) n = A,T,C or G 9 gtccactctc ctttgagtgt actgtcttac tgtgcactct gtttttcaac tttctagata 60 taaaaaatgc ttgttctata gtggagtaag agctcacaca cccaaggcag caagataact 120 gaaaaaagcg aggctttttt gccaccttgg taaaggccag ttcactgcta tagaactgct 180 ataagcctga agggaagtag ctatgagact ttccattttt cttagttctc ccaataggct 240 ccttcatgga aaaaggcttc ctgtaataat tttcacctaa tgaattagca gtgtgattat 300 ttctgaaata agagacaaat tgggccgcag agtcttcctg tgatttaaaa taaacaaccc 360 aaagttttgt ttggtcttca ccaaaggaca tactctaggg ggtatgttgt tgaagacatt 420 caaaaacatt agctgttctg tctttcaatt tcaagttatt ttggagactg cctccatgtg 480 agttaattac tttgctctgg aactagcatt attgtcatta tcatcacatt ctgtcatcat 540 catctgaata atattgtgga tttccccctc tgcttgcatc ttcttttgac tcctctggga 600 anaaatgtca aaaaaaaagg tcgatctact cngcaaggnc catctaatca ctgcgctgga 660 aggacccnct gccc 674 10 346 DNA Homo sapien misc_feature (1)...(346) n = A,T,C or G 10 actagtctgc tgatagaaag cactatacat cctattgttt ctttctttcc aaaatcagcc 60 ttctgtctgt aacaaaaatg tactttatag agatggagga aaaggtctaa tactacatag 120 ccttaagtgt ttctgtcatt gttcaagtgt attttctgta acagaaacat atttggaatg 180 tttttctttt ccccttataa attgtaattc ctgaaatact gctgctttaa aaagtcccac 240 tgtcagatta tattatctaa caattgaata ttgtaaatat acttgtctta cctctcaata 300 aaagggtact tttctattan nnagnngnnn gnnnnataaa anaaaa 346 11 602 DNA Homo sapien 11 actagtaaaa agcagcattg ccaaataatc cctaattttc cactaaaaat ataatgaaat 60 gatgttaagc tttttgaaaa gtttaggtta aacctactgt tgttagatta atgtatttgt 120 tgcttccctt tatctggaat gtggcattag cttttttatt ttaaccctct ttaattctta 180 ttcaattcca tgacttaagg ttggagagct aaacactggg atttttggat aacagactga 240 cagttttgca taattataat cggcattgta catagaaagg atatggctac cttttgttaa 300 atctgcactt tctaaatatc aaaaaaggga aatgaagtta taaatcaatt tttgtataat 360 ctgtttgaaa catgagtttt atttgcttaa tattagggct ttgccccttt tctgtaagtc 420 tcttgggatc ctgtgtagaa ctgttctcat taaacaccaa acagttaagt ccattctctg 480 gtactagcta caaattcggt ttcatattct acttaacaat ttaaataaac tgaaatattt 540 ctagatggtc tacttctgtt catataaaaa caaaacttga tttccaaaaa aaaaaaaaaa 600 aa 602 12 685 DNA Homo sapien misc_feature (1)...(685) n = A,T,C or G 12 actagtcctg tgaaagtaca actgaaggca gaaagtgtta ggattttgca tctaatgttc 60 attatcatgg tattgatgga cctaagaaaa taaaaattag actaagcccc caaataagct 120 gcatgcattt gtaacatgat tagtagattt gaatatatag atgtagtatn ttgggtatct 180 aggtgtttta tcattatgta aaggaattaa agtaaaggac tttgtagttg tttttattaa 240 atatgcatat agtagagtgc aaaaatatag caaaaatana aactaaaggt agaaaagcat 300 tttagatatg ccttaatnta nnaactgtgc caggtggccc tcggaataga tgccaggcag 360 agaccagtgc ctgggtggtg cctccccttg tctgcccccc tgaagaactt ccctcacgtg 420 angtagtgcc ctcgtaggtg tcacgtggan tantggganc aggccgnncn gtnanaagaa 480 ancanngtga nagtttcncc gtngangcng aactgtccct gngccnnnac gctcccanaa 540 cntntccaat ngacaatcga gtttccnnnc tccngnaacc tngccgnnnn cnngcccnnc 600 cantntgnta accccgcgcc cggatcgctc tcnnntcgtt ctcncncnaa ngggntttcn 660 cnnccgccgt cncnnccccg cnncc 685 13 694 DNA Homo sapien misc_feature (1)...(694) n = A,T,C or G 13 cactagtcac tcattagcgt tttcaatagg gctcttaagt ccagtagatt acgggtagtc 60 agttgacgaa gatctggttt acaagaacta attaaatgtt tcattgcatt tttgtaagaa 120 cagaataatt ttataaaatg tttgtagttt ataattgccg aaaataattt aaagacactt 180 tttctctgtg tgtgcaaatg tgtgtttgtg atccattttt tttttttttt taggacacct 240 gtttactagc tagctttaca atatgccaaa aaaggatttc tccctgaccc catccgtggt 300 tcaccctctt ttccccccat gctttttgcc ctagtttata acaaaggaat gatgatgatt 360 taaaaagtag ttctgtatct tcagtatctt ggtcttccag aaccctctgg ttgggaaggg 420 gatcattttt tactggtcat ttccctttgg agtgtactac tttaacagat ggaaagaact 480 cattggccat ggaaacagcc gangtgttgg gagccagcag tgcatggcac cgtccggcat 540 ctggcntgat tggtctggct gccgtcattg tcagcacagt gccatgggac atggggaana 600 ctgactgcac ngccaatggt tttcatgaag aatacngcat ncncngtgat cacgtnancc 660 angacgctat gggggncana gggccanttg cttc 694 14 679 DNA Homo sapien misc_feature (1)...(679) n = A,T,C or G 14 cagccgcctg catctgtatc cagcgccang tcccgccagt cccagctgcg cgcgcccccc 60 agtcccgnac ccgttcggcc cangctnagt tagncctcac catnccggtc aaaggangca 120 ccaagtgcat caaatacctg cngtncggat ntaaattcat cttctggctt gccgggattg 180 ctgtccntgc cattggacta nggctccgat ncgactctca gaccanganc atcttcganc 240 naganactaa tnatnattnt tccagcttct acacaggagt ctatattctg atcggatccg 300 gcnccctcnt gatgctggtg ggcttcctga gctgctgcgg ggctgtgcaa gagtcccant 360 gcatgctggg actgttcttc ggcttcntct tggtgatatn cgccattgaa atacctgcgg 420 ccatctgggg atattccact ncgatnatgt gattaaggaa ntccacggag ttttacaagg 480 acacgtacaa cnacctgaaa accnnggatg anccccaccg ggaancnctg aangccatcc 540 actatgcgtt gaactgcaat ggtttggctg gggnccttga acaatttaat cncatacatc 600 tggccccann aaaggacntn ctcganncct tcnccgtgna attcngttct gatnccatca 660 cagaagtctc gaacaatcc 679 15 695 DNA Homo sapien misc_feature (1)...(695) n = A,T,C or G 15 actagtggat aaaggccagg gatgctgctc aacctcctac catgtacagg gacgtctccc 60 cattacaact acccaatccg aagtgtcaac tgtgtcagga ctaanaaacc ctggttttga 120 ttaaaaaagg gcctgaaaaa aggggagcca caaatctgtc tgcttcctca cnttantcnt 180 tggcaaatna gcattctgtc tcnttggctg cngcctcanc ncaaaaaanc ngaactcnat 240 cnggcccagg aatacatctc ncaatnaacn aaattganca aggcnntggg aaatgccnga 300 tgggattatc ntccgcttgt tgancttcta agtttcnttc ccttcattcn accctgccag 360 ccnagttctg ttagaaaaat gccngaattc naacnccggt tttcntactc ngaatttaga 420 tctncanaaa cttcctggcc acnattcnaa ttnanggnca cgnacanatn ccttccatna 480 ancncacccc acntttgana gccangacaa tgactgcntn aantgaaggc ntgaaggaan 540 aactttgaaa ggaaaaaaaa ctttgtttcc ggccccttcc aacncttctg tgttnancac 600 tgccttctng naaccctgga agcccngnga cagtgttaca tgttgttcta nnaaacngac 660 ncttnaatnt cnatcttccc nanaacgatt ncncc 695 16 669 DNA Homo sapien misc_feature (1)...(669) n = A,T,C or G 16 cgccgaagca gcagcgcagg ttgtccccgt ttcccctccc ccttcccttc tccggttgcc 60 ttcccgggcc ccttacactc cacagtcccg gtcccgccat gtcccagaaa caagaagaag 120 agaaccctgc ggaggagacc ggcgaggaga agcaggacac gcaggagaaa gaaggtattc 180 tgcctgagag agctgaagag gcaaagctaa aggccaaata cccaagccta ggacaaaagc 240 ctggaggctc cgacttcctc atgaagagac tccagaaagg gcaaaagtac tttgactcng 300 gagactacaa catggccaaa gccaacatga agaataagca gctgccaagt gcangaccag 360 acaagaacct ggtgactggt gatcacatcc ccaccccaca ggatctgccc agagaaagtc 420 ctcgctcgtc accagcaagc ttgcgggtgg ccaagttgaa tgatgctgcc ggggctctgc 480 canatctgag acgcttccct ccctgcccca cccgggtcct gtgctggctc ctgcccttcc 540 tgcttttgca gccangggtc aggaagtggc ncnggtngtg gctggaaagc aaaacccttt 600 cctgttggtg tcccacccat ggagcccctg gggcgagccc angaacttga ncctttttgt 660 tntcttncc 669 17 697 DNA Homo sapien misc_feature (1)...(697) n = A,T,C or G 17 gcaagatatg gacaactaag tgagaaggta atnctctact gctctagntn ctccnggcnn 60 gacgcgctga ggagannnac gctggcccan ctgccggcca cacacgggga tcntggtnat 120 gcctgcccan gggancccca ncnctcggan cccatntcac acccgnnccn tncgcccacn 180 ncctggctcn cncngcccng nccagctcnc gnccccctcc gccnnnctcn ttnncntctc 240 cncnccctcc ncnacnacct cctacccncg gctccctccc cagccccccc ccgcaancct 300 ccacnacncc ntcnncncga ancnccnctc gcnctcngcc ccngccccct gccccccgcc 360 cncnacnncg cgntcccccg cgcncgcngc ctcnccccct cccacnacag ncncacccgc 420 agncacgcnc tccgcccnct gacgccccnn cccgccgcgc tcaccttcat ggnccnacng 480 ccccgctcnc nccnctgcnc gccgncnngg cgccccgccc cnnccgngtn ccncncgnng 540 ccccngcngn angcngtgcg cnncangncc gngccgnncn ncaccctccg nccnccgccc 600 cgcccgctgg gggctcccgc cncgcggntc antccccncc cntncgccca ctntccgntc 660 cnncnctcnc gctcngcgcn cgcccnccnc ccccccc 697 18 670 DNA Homo sapien misc_feature (1)...(670) n = A,T,C or G 18 ctcgtgtgaa gggtgcagta cctaagccgg agcggggtag aggcgggccg gcaccccctt 60 ctgacctcca gtgccgccgg cctcaagatc agacatggcc cagaacttga acgacttggc 120 gggacggctg cccgccgggc cccggggcat gggcacggcc ctgaagctgt tgctgggggc 180 cggcgccgtg gcctacggtg tgcgcgaatc tgtgttcacc gtggaaggcg ggcncagagc 240 catcttcttc aatcggatcg gtggagtgca caggacacta tcctgggccg anggccttca 300 cttcaggatc cttggttcca gtaccccanc atctatgaca ttcgggccag acctcgaaaa 360 aatctcctcc ctacaggctc caaagaccta cagatggtga atatctccct gcgagtgttg 420 tctcgaccaa tgctcangaa cttcctaaca tgttccancg cctaagggct ggactacnaa 480 gaacgantgt tgccgtccat tgtcacgaag tgctcaagaa tttnggtggc caagttcaat 540 gncctcacnn ctgatcnccc agcggggcca agttanccct ggttgatccc cgggganctg 600 acnnaaaagg gccaaggact tcccctcatc ctggataatg tggccntcac aaagctcaac 660 tttanccacc 670 19 606 DNA Homo sapien misc_feature (1)...(606) n = A,T,C or G 19 actagtgcca acctcagctc ccaggccagt tctctgaatg tcgaggagtt ccaggatctc 60 tggcctcagt tgtccttggt tattgatggg ggacaaattg gggatggcca gagccccgag 120 tgtcgccttg gctcaactgt ggttgatttg tctgtgcccg gaaagtttgg catcattcgt 180 ccaggctgtg ccctggaaag tactacagcc atcctccaac agaagtacgg actgctcccc 240 tcacatgcgt cctacctgtg aaactctggg aagcaggaag gcccaagacc tggtgctgga 300 tactatgtgt ctgtccactg acgactgtca aggcctcatt tgcagaggcc accggagcta 360 gggcactagc ctgactttta aggcagtgtg tctttctgag cactgtagac caagcccttg 420 gagctgctgg tttagccttg cacctgggga aaggatgtat ttatttgtat tttcatatat 480 cagccaaaag ctgaatggaa aagttnagaa cattcctagg tggccttatt ctaataagtt 540 tcttctgtct gttttgtttt tcaattgaaa agttattaaa taacagattt agaatctagt 600 gagacc 606 20 449 DNA Homo sapien 20 actagtaaac aacagcagca gaaacatcag tatcagcagc gtcgccagca ggagaatatg 60 cagcgccaga gccgaggaga acccccgctc cctgaggagg acctgtccaa actcttcaaa 120 ccaccacagc cgcctgccag gatggactcg ctgctcattg caggccagat aaacacttac 180 tgccagaaca tcaaggagtt cactgcccaa aacttaggca agctcttcat ggcccaggct 240 cttcaagaat acaacaacta agaaaaggaa gtttccagaa aagaagttaa catgaactct 300 tgaagtcaca ccagggcaac tcttggaaga aatatatttg catattgaaa agcacagagg 360 atttctttag tgtcattgcc gattttggct ataacagtgt ctttctagcc ataataaaat 420 aaaacaaaat cttgactgct tgctcaaaa 449 21 409 DNA Homo sapien 21 tatcaatcaa ctggtgaata attaaacaat gtgtggtgtg atcatacaaa gggtaccact 60 caatgataaa aggaacaagc tgcctatatg tggaacaaca tggatgcatt tcagaaactt 120 tatgttgagt gaaagaacaa acacggagaa catactatgt ggttctcttt atgtaacatt 180 acagaaataa aaacagaggc aaccaccttt gaggcagtat ggagtgagat agactggaaa 240 aaggaaggaa ggaaactcta cgctgatgga aatgtctgtg tcttcattgg gtggtagtta 300 tgtggggata tacatttgtc aaaatttatt gaactatata ctaaagaact ctgcatttta 360 ttgggatgta aataatacct caattaaaaa gacaaaaaaa aaaaaaaaa 409 22 649 DNA Homo sapien misc_feature (1)...(649) n = A,T,C or G 22 acaattttca ttatcttaag cacattgtac atttctacag aacctgtgat tattctcgca 60 tgataaggat ggtacttgca tatggtgaat tactactgtt gacagtttcc gcagaaatcc 120 tatttcagtg gaccaacatt gtggcatggc agcaaatgcc aacattttgt ggaatagcag 180 caaatctaca agagaccctg gttggttttt cgttttgttt tctttgtttt ttcccccttc 240 tcctgaatca gcagggatgg aangagggta gggaagttat gaattactcc ttccagtagt 300 agctctgaag tgtcacattt aatatcagtt ttttttaaac atgattctag ttnaatgtag 360 aagagagaag aaagaggaag tgttcacttt tttaatacac tgatttagaa atttgatgtc 420 ttatatcagt agttctgagg tattgatagc ttgctttatt tctgccttta cgttgacagt 480 gttgaagcag ggtgaataac taggggcata tatatttttt ttttttgtaa gctgtttcat 540 gatgttttct ttggaatttc cggataagtt caggaaaaca tctgcatgtt gttatctagt 600 ctgaagttcn tatccatctc attacaacaa aaacncccag aacggnttg 649 23 669 DNA Homo sapien misc_feature (1)...(669) n = A,T,C or G 23 actagtgccg tactggctga aatccctgca ggaccaggaa gagaaccagt tcagactttg 60 tactctcagt caccagctct ggaattagat aaattccttg aagatgtcag gaatgggatc 120 tatcctctga cagcctttgg gctgcctcgg ccccagcagc cacagcagga ggaggtgaca 180 tcacctgtcg tgcccccctc tgtcaagact ccgacacctg aaccagctga ggtggagact 240 cgcaaggtgg tgctgatgca gtgcaacatt gagtcggtgg aggagggagt caaacaccac 300 ctgacacttc tgctgaagtt ggaggacaaa ctgaaccggc acctgagctg tgacctgatg 360 ccaaatgaga atatccccga gttggcggct gagctggtgc agctgggctt cattagtgag 420 gctgaccaga gccggttgac ttctctgcta gaagagactt gaacaagttc aattttgcca 480 ggaacagtac cctcaactca gccgctgtca ccgtctcctc ttagagctca ctcgggccag 540 gccctgatct gcgctgtggc tgtcctggac gtgctgcacc ctctgtcctt ccccccagtc 600 agtattacct gtgaagccct tccctccttt attattcagg anggctgggg gggctccttg 660 nttctaacc 669 24 442 DNA Homo sapien 24 actagtacca tcttgacaga ggatacatgc tcccaaaacg tttgttacca cacttaaaaa 60 tcactgccat cattaagcat cagtttcaaa attatagcca ttcatgattt actttttcca 120 gatgactatc attattctag tcctttgaat ttgtaagggg aaaaaaaaca aaaacaaaaa 180 cttacgatgc acttttctcc agcacatcag atttcaaatt gaaaattaaa gacatgctat 240 ggtaatgcac ttgctagtac tacacacttt ggtacaacaa aaaacagagg caagaaacaa 300 cggaaagaga aaagccttcc tttgttggcc cttaaactga gtcaagatct gaaatgtaga 360 gatgatctct gacgatacct gtatgttctt attgtgtaaa taaaattgct ggtatgaaat 420 gacctaaaaa aaaaaaaaga aa 442 25 656 DNA Homo sapien misc_feature (1)...(656) n = A,T,C or G 25 tgcaagtacc acacactgtt tgaattttgc acaaaaagtg actgtaggat caggtgatag 60 ccccggaatg tacagtgtct tggtgcacca agatgccttc taaaggctga cataccttgg 120 accctaatgg ggcagagagt atagccctag cccagtggtg acatgaccac tccctttggg 180 aggcctgagg tagaggggag tggtatgtgt tttctcagtg gaagcagcac atgagtgggt 240 gacaggatgt tagataaagg ctctagttag ggtgtcattg tcatttgaga gactgacaca 300 ctcctagcag ctggtaaagg ggtgctggan gccatggagg anctctagaa acattagcat 360 gggctgatct gattacttcc tggcatcccg ctcactttta tgggaagtct tattagangg 420 atgggacagt tttccatatc cttgctgtgg agctctggaa cactctctaa atttccctct 480 attaaaaatc actgccctaa ctacacttcc tccttgaagg aatagaaatg gaactttctc 540 tgacatantt cttggcatgg ggagccagcc acaaatgana atctgaacgt gtccaggttt 600 ctcctganac tcatctacat agaattggtt aaaccctccc ttggaataag gaaaaa 656 26 434 DNA Homo sapien misc_feature (1)...(434) n = A,T,C or G 26 actagttcag actgccacgc caaccccaga aaatacccca catgccagaa aagtgaagtc 60 ctaggtgttt ccatctatgt ttcaatctgt ccatctacca ggcctcgcga taaaaacaaa 120 acaaaaaaac gctgccaggt tttagaagca gttctggtct caaaaccatc aggatcctgc 180 caccagggtt cttttgaaat agtaccacat gtaaaaggga atttggcttt cacttcatct 240 aataactgaa ttgtcaggct ttgattgata attgtagaaa taagtagcct tctgttgtgg 300 gaataagtta taatcagtat tcatctcttt gttttttgtc actcttttct ctctaattgt 360 gtcatttgta ctgtttgaaa aatatttctt ctatnaaatt aaactaacct gccttaaaaa 420 aaaaaaaaaa aaaa 434 27 654 DNA Homo sapien misc_feature (1)...(654) n = A,T,C or G 27 actagtccaa cacagtcaga aacattgttt tgaatcctct gtaaaccaag gcattaatct 60 taataaacca ggatccattt aggtaccact tgatataaaa aggatatcca taatgaatat 120 tttatactgc atcctttaca ttagccacta aatacgttat tgcttgatga agacctttca 180 cagaatccta tggattgcag catttcactt ggctacttca tacccatgcc ttaaagaggg 240 gcagtttctc aaaagcagaa acatgccgcc agttctcaag ttttcctcct aactccattt 300 gaatgtaagg gcagctggcc cccaatgtgg ggaggtccga acattttctg aattcccatt 360 ttcttgttcg cggctaaatg acagtttctg tcattactta gattccgatc tttcccaaag 420 gtgttgattt acaaagaggc cagctaatag cagaaatcat gaccctgaaa gagagatgaa 480 attcaagctg tgagccaggc agganctcag tatggcaaag gtcttgagaa tcngccattt 540 ggtacaaaaa aaattttaaa gcntttatgt tataccatgg aaccatagaa anggcaaggg 600 aattgttaag aanaatttta agtgtccaga cccanaanga aaaaaaaaaa aaaa 654 28 670 DNA Homo sapien misc_feature (1)...(670) n = A,T,C or G 28 cgtgtgcaca tactgggagg atttccacag ctgcacggtc acagccctta cggattgcca 60 ggaaggggcg aaagatatgt gggataaact gagaaaagaa nccaaaaacc tcaacatcca 120 aggcagctta ttcgaactct gcggcagcgg caacggggcg gcggggtccc tgctcccggc 180 gttcccggtg ctcctggtgt ctctctcggc agctttagcg acctgncttt ccttctgagc 240 gtggggccag ctccccccgc ggcgcccacc cacnctcact ccatgctccc ggaaatcgag 300 aggaagatca ttagttcttt ggggacgttn gtgattctct gtgatgctga aaaacactca 360 tatagggaat gtgggaaatc ctganctctt tnttatntcg tntgatttct tgtgttttat 420 ttgccaaaat gttaccaatc agtgaccaac cnagcacagc caaaaatcgg acntcngctt 480 tagtccgtct tcacacacag aataagaaaa cggcaaaccc accccacttt tnantttnat 540 tattactaan ttttttctgt tgggcaaaag aatctcagga acngccctgg ggccnccgta 600 ctanagttaa ccnagctagt tncatgaaaa atgatgggct ccncctcaat gggaaagcca 660 agaaaaagnc 670 29 551 DNA Homo sapien misc_feature (1)...(551) n = A,T,C or G 29 actagtcctc cacagcctgt gaatccccct agacctttca agcatagtga gcggagaaga 60 agatctcagc gtttagccac cttacccatg cctgatgatt ctgtagaaaa ggtttcttct 120 ccctctccag ccactgatgg gaaagtattc tccatcagtt ctcaaaatca gcaagaatct 180 tcagtaccag aggtgcctga tgttgcacat ttgccacttg agaagctggg accctgtctc 240 cctcttgact taagtcgtgg ttcagaagtt acagcaccgg tagcctcaga ttcctcttac 300 cgtaatgaat gtcccagggc agaaaaagag gatacncaga tgcttccaaa tccttcttcc 360 aaagcaatag ctgatgggaa gaggagctcc agcagcagca ggaatatcga aaacagaaaa 420 aaaagtgaaa ttgggaagac aaaagctcaa cagcatttgg taaggagaaa aganaagatg 480 aggaaggaag agagaagaga gacnaagatc nctacggacc gnnncggaag aagaagaagn 540 aaaaaanaaa a 551 30 684 DNA Homo sapien misc_feature (1)...(684) n = A,T,C or G 30 actagttcta tctggaaaaa gcccgggttg gaagaagctg tggagagtgc gtgtgcaatg 60 cgagactcat ttcttggaag catccctggc aaaaatgcag ctgagtacaa ggttatcact 120 gtgatagaac ctggactgct ttttgagata atagagatgc tgcagtctga agagacttcc 180 agcacctctc agttgaatga attaatgatg gcttctgagt caactttact ggctcaggaa 240 ccacgagaga tgactgcaga tgtaatcgag cttaaaggga aattcctcat caacttagaa 300 ggtggtgata ttcgtgaaga gtcttcctat aaagtaattg tcatgccgac tacgaaagaa 360 aaatgccccc gttgttggaa gtatacagcg ggagtcttca gatacactgt gtcctcgatg 420 tgcagaagtt gtcagtggga aaatagtatt aacagctcac tcgagcaaga accctcctga 480 cagtactggg ctagaagttt ggatggatta tttacaatat aggaaagaaa gccaagaatt 540 aggtnatgag tggatgagta aatggtggan gatggggaat tcaaatcaga attatggaag 600 aagttnttcc tgttactata gaaaggaatt atgtttattt acatgcagaa aatatanatg 660 tgtggtgtgt accgtggatg gaan 684 31 654 DNA Homo sapien misc_feature (1)...(654) n = A,T,C or G 31 gcgcagaaaa ggaaccaata tttcagaaac aagcttaata ggaacagctg cctgtacatc 60 aacatcttct cagaatgacc cagaagttat catcgtggga gctggcgtgc ttggctctgc 120 tttggcagct gtgctttcca gagatggaag aaaggtgaca gtcattgaga gagacttaaa 180 agagcctgac agaatagttg gagaattcct gcagccgggt ggttatcatg ttctcaaaga 240 ccttggtctt ggagatacag tggaaggtct tgatgcccag gttgtaaatg gttacatgat 300 tcatgatcag ggaaagcaaa tcagangttc agattcctta ccctctgtca gaaaacaatc 360 aagtgcagag tggaagagct ttccatcacg gaagattcat catgagtctc cggaaagcag 420 ctatggcaga gcccaatgca aagtttattg aaggtgttgt gttacagtta ttagaggaag 480 atgatgttgt gatgggagtt cagtacaagg ataaagagac tgggagatat caaggaactc 540 catgctccac tgactgttgt tgcagatggg cttttctcca anttcaggaa aagcctggtc 600 tcaataaagt ttctgtatca ctcatttggt tggcttctta tgaagaatgc nccc 654 32 673 DNA Homo sapien misc_feature (1)...(673) n = A,T,C or G 32 actagtgaag aaaaagaaat tctgatacgg gacaaaaatg ctcttcaaaa catcattctt 60 tatcacctga caccaggagt tttcattgga aaaggatttg aacctggtgt tactaacatt 120 ttaaagacca cacaaggaag caaaatcttt ctgaaagaag taaatgatac acttctggtg 180 aatgaattga aatcaaaaga atctgacatc atgacaacaa atggtgtaat tcatgttgta 240 gataaactcc tctatccagc agacacacct gttggaaatg atcaactgct ggaaatactt 300 aataaattaa tcaaatacat ccaaattaag tttgttcgtg gtagcacctt caaagaaatc 360 cccgtgactg tctatnagcc aattattaaa aaatacacca aaatcattga tgggagtgcc 420 tgtgggaaat aactgaaaaa gagaccgaga agaacgaatc attacaggtc ctgaaataaa 480 atacctagga tttctactgg aggtggagaa acagaagaac tctgaagaaa ttgttacaag 540 aagangtccc aaggtcacca aattcattga aggtggtgat ggtctttatt tgaagatgaa 600 gaaattaaaa gacgcttcag ggagacnccc catgaaggaa ttgccagcca caaaaaaatt 660 cagggattag aaa 673 33 673 DNA Homo sapien misc_feature (1)...(673) n = A,T,C or G 33 actagttatt tactttcctc cgcttcagaa ggtttttcag actgagagcc taagcatact 60 ggatctgttg tttcttttgg gtctcacctc atcagtgtgc atagtggcag aaattataaa 120 gaaggttgaa aggagcaggg aaaagatcca gaagcatgtt agttcgacat catcatcttt 180 tcttgaagta tgatgcatat tgcattattt tatttgcaaa ctaggaattg cagtctgagg 240 atcatttaga agggcaagtt caagaggata tgaagatttg agaacttttt aactattcat 300 tgactaaaaa tgaacattaa tgttnaagac ttaagacttt aacctgctgg cagtcccaaa 360 tgaaattatg caactttgat atcatattcc ttgatttaaa ttgggctttt gtgattgant 420 gaaactttat aaagcatatg gtcagttatt tnattaaaaa ggcaaaacct gaaccacctt 480 ctgcacttaa agaagtctaa cagtacaaat acctatctat cttagatgga tntatttntt 540 tntattttta aatattgtac tatttatggt nggtggggct ttcttactaa tacacaaatn 600 aatttatcat ttcaanggca ttctatttgg gtttagaagt tgattccaag nantgcatat 660 ttcgctactg tnt 673 34 684 DNA Homo sapien misc_feature (1)...(684) n = A,T,C or G 34 actagtttat tcaagaaaag aacttactga ttcctctgtt cctaaagcaa gagtggcagg 60 tgatcagggc tggtgtagca tccggttcct ttagtgcagc taactgcatt tgtcactgat 120 gaccaaggag gaaatcacta agacatttga gaagcagtgg tatgaacgtt cttggacaag 180 ccacagttct gagccttaac cctgtagttt gcacacaaga acgagctcca cctccccttc 240 ttcaggagga atctgtgcgg atagattggc tggacttttc aatggttctg ggttgcaagt 300 gggcactgtt atggctgggt atggagcgga cagccccagg aatcagagcc tcagcccggc 360 tgcctggttg gaaggtacag gtgttcagca ccttcggaaa aagggcataa agtngtgggg 420 gacaattctc agtccaagaa gaatgcattg accattgctg gctatttgct tncctagtan 480 gaattggatn catttttgac cangatnntt ctnctatgct ttnttgcaat gaaatcaaat 540 cccgcattat ctacaagtgg tatgaagtcc tgcnnccccc agagaggctg ttcaggcnat 600 gtcttccaag ggcagggtgg gttacaccat tttacctccc ctctcccccc agattatgna 660 cncagaagga atttntttcc tccc 684 35 614 DNA Homo sapien misc_feature (1)...(614) n = A,T,C or G 35 actagtccaa cgcgttngcn aatattcccc tggtagccta cttccttacc cccgaatatt 60 ggtaagatcg agcaatggct tcaggacatg ggttctcttc tcctgtgatc attcaagtgc 120 tcactgcatg aagactggct tgtctcagtg tntcaacctc accagggctg tctcttggtc 180 cacacctcgc tccctgttag tgccgtatga cagcccccat canatgacct tggccaagtc 240 acggtttctc tgtggtcaat gttggtnggc tgattggtgg aaagtanggt ggaccaaagg 300 aagncncgtg agcagncanc nccagttctg caccagcagc gcctccgtcc tactngggtg 360 ttccngtttc tcctggccct gngtgggcta nggcctgatt cgggaanatg cctttgcang 420 gaaggganga taantgggat ctaccaattg attctggcaa aacnatntct aagattnttn 480 tgctttatgt ggganacana tctanctctc atttnntgct gnanatnaca ccctactcgt 540 gntcgancnc gtcttcgatt ttcgganaca cnccantnaa tactggcgtt ctgttgttaa 600 aaaaaaaaaa aaaa 614 36 686 DNA Homo sapien misc_feature (1)...(686) n = A,T,C or G 36 gtggctggcc cggttctccg cttctcccca tcccctactt tcctccctcc ctccctttcc 60 ctccctcgtc gactgttgct tgctggtcgc agactccctg acccctccct cacccctccc 120 taacctcggt gccaccggat tgcccttctt ttcctgttgc ccagcccagc cctagtgtca 180 gggcgggggc ctggagcagc ccgaggcact gcagcagaag ananaaaaga cacgacnaac 240 ctcagctcgc cagtccggtc gctngcttcc cgccgcatgg caatnagaca gacgccgctc 300 acctgctctg ggcacacgcg acccgtggtt gatttggcct tcagtggcat cacccttatg 360 ggtatttctt aatcagcgct tgcaaagatg gttaacctat gctacgccag ggagatacag 420 gagactggat tggaacattt ttggggtcta aaggtctgtt tggggtgcaa cactgaataa 480 ggatgccacc aaagcagcta cagcagctgc agatttcaca gcccaagtgt gggatgctgt 540 ctcagganat naattgataa cctggctcat aacacattgt caagaatgtg gatttcccca 600 ggatattatt atttgtttac cggggganag gataactgtt tcncntattt taattgaaca 660 aactnaaaca aaanctaagg aaatcc 686 37 681 DNA Homo sapien misc_feature (1)...(681) n = A,T,C or G 37 gagacanacn naacgtcang agaanaaaag angcatggaa cacaanccag gcncgatggc 60 caccttccca ccagcancca gcgcccccca gcngccccca ngnccggang accangactc 120 cancctgnat caatctganc tctattcctg gcccatncct acctcggagg tggangccgn 180 aaaggtcgca cnnncagaga agctgctgcc ancaccancc gccccnnccc tgncgggctn 240 nataggaaac tggtgaccnn gctgcanaat tcatacagga gcacgcgang ggcacnnnct 300 cacactgagt tnnngatgan gcctnaccan ggacctnccc cagcnnattg annacnggac 360 tgcggaggaa ggaagacccc gnacnggatc ctggccggcn tgccaccccc ccacccctag 420 gattatnccc cttgactgag tctctgaggg gctacccgaa cccgcctcca ttccctacca 480 natnntgctc natcgggact gacangctgg ggatnggagg ggctatcccc cancatcccc 540 tnanaccaac agcnacngan natnggggct ccccngggtc ggngcaacnc tcctncaccc 600 cggcgcnggc cttcggtgnt gtcctccntc aacnaattcc naaanggcgg gccccccngt 660 ggactcctcn ttgttccctc c 681 38 687 DNA Homo sapien misc_feature (1)...(687) n = A,T,C or G 38 canaaaaaaa aaaacatggc cgaaaccagn aagctgcgcg atggcgccac ggcccctctt 60 ctcccggcct gtgtccggaa ggtttccctc cgaggcgccc cggctcccgc aagcggagga 120 gagggcggga cntgccgggg ccggagctca naggccctgg ggccgctctg ctctcccgcc 180 atcgcaaggg cggcgctaac ctnaggcctc cccgcaaagg tccccnangc ggnggcggcg 240 gggggctgtg anaaccgcaa aaanaacgct gggcgcgcng cgaacccgtc cacccccgcg 300 aaggananac ttccacagan gcagcgtttc cacagcccan agccacnttt ctagggtgat 360 gcaccccagt aagttcctgn cggggaagct caccgctgtc aaaaaanctc ttcgctccac 420 cggcgcacna aggggangan ggcangangc tgccgcccgc acaggtcatc tgatcacgtc 480 gcccgcccta ntctgctttt gtgaatctcc actttgttca accccacccg ccgttctctc 540 ctccttgcgc cttcctctna ccttaanaac cagcttcctc tacccnatng tanttnctct 600 gcncnngtng aaattaattc ggtccnccgg aacctcttnc ctgtggcaac tgctnaaaga 660 aactgctgtt ctgnttactg cngtccc 687 39 695 DNA Homo sapien misc_feature (1)...(695) n = A,T,C or G 39 actagtctgg cctacaatag tgtgattcat gtaggacttc tttcatcaat tcaaaacccc 60 tagaaaaacg tatacagatt atataagtag ggataagatt tctaacattt ctgggctctc 120 tgacccctgc gctagactgt ggaaagggag tattattata gtatacaaca ctgctgttgc 180 cttattagtt ataacatgat aggtgctgaa ttgtgattca caatttaaaa acactgtaat 240 ccaaactttt ttttttaact gtagatcatg catgtgaatg ttaatgttaa tttgttcaan 300 gttgttatgg gtagaaaaaa ccacatgcct taaaatttta aaaagcaggg cccaaactta 360 ttagtttaaa attaggggta tgtttccagt ttgttattaa ntggttatag ctctgtttag 420 aanaaatcna ngaacangat ttngaaantt aagntgacat tatttnccag tgacttgtta 480 atttgaaatc anacacggca ccttccgttt tggtnctatt ggnntttgaa tccaancngg 540 ntccaaatct tnttggaaac ngtccnttta acttttttac nanatcttat ttttttattt 600 tggaatggcc ctatttaang ttaaaagggg ggggnnccac naccattcnt gaataaaact 660 naatatatat ccttggtccc ccaaaattta aggng 695 40 674 DNA Homo sapien misc_feature (1)...(674) n = A,T,C or G 40 actagtagtc agttgggagt ggttgctata ccttgacttc atttatatga atttccactt 60 tattaaataa tagaaaagaa aatcccggtg cttgcagtag agttatagga cattctatgc 120 ttacagaaaa tatagccatg attgaaatca aatagtaaag gctgttctgg ctttttatct 180 tcttagctca tcttaaataa gtagtacact tgggatgcag tgcgtctgaa gtgctaatca 240 gttgtaacaa tagcacaaat cgaacttagg atgtgtttct tctcttctgt gtttcgattt 300 tgatcaattc tttaattttg ggaacctata atacagtttt cctattcttg gagataaaaa 360 ttaaatggat cactgatatt taagtcattc tgcttctcat ctnaatattc catattctgt 420 attagganaa antacctccc agcacagccc cctctcaaac cccacccaaa accaagcatt 480 tggaatgagt ctcctttatt tccgaantgt ggatggtata acccatatcn ctccaatttc 540 tgnttgggtt gggtattaat ttgaactgtg catgaaaagn ggnaatcttt nctttgggtc 600 aaantttncc ggttaatttg nctngncaaa tccaatttnc tttaagggtg tctttataaa 660 atttgctatt cngg 674 41 657 DNA Homo sapien misc_feature (1)...(657) n = A,T,C or G 41 gaaacatgca agtaccacac actgtttgaa ttttgcacaa aaagtgactg tagggatcag 60 gtgatagccc cggaatgtac agtgtcttgg tgcaccaaga tgccttctaa aggctgacat 120 accttgggac cctaatgggg cagagagtat agccctagcc cagtggtgac atgaccactc 180 cctttgggag gctgaagtta aagggaatgg tatgtgtttt ctcatggaag cagcacatga 240 atnggtnaca ngatgttaaa ntaaggntct antttgggtg tcttgtcatt tgaaaaantg 300 acacactcct ancanctggt aaaggggtgc tggaagccat ggaagaactc taaaaacatt 360 agcatgggct gatctgatta cttcctggca tcccgctcac ttttatggga agtcttatta 420 naaggatggg ananttttcc atatccttgc tgttggaact ctggaacact ctctaaattt 480 ccctctatta aaaatcactg nccttactac acttcctcct tganggaata gaaatggacc 540 tttctctgac ttagttcttg gcatggganc cagcccaaat taaaatctga cttntccggt 600 ttctccngaa ctcacctact tgaattggta aaacctcctt tggaattagn aaaaacc 657 42 389 DNA Homo sapien misc_feature (1)...(389) n = A,T,C or G 42 actagtgctg aggaatgtaa acaagtttgc tgggccttgc gagacttcac caggttgttt 60 cgatagctca cactcctgca ctgtgcctgt cacccaggaa tgtctttttt aattagaaga 120 caggaagaaa acaaaaacca gactgtgtcc cacaatcaga aacctccgtt gtggcagang 180 ggccttcacc gccaccaggg tgtcccgcca gacagggaga gactccagcc ttctgaggcc 240 atcctgaaga attcctgttt gggggttgtg aaggaaaatc acccggattt aaaaagatgc 300 tgttgcctgc ccgcgtngtn gggaagggac tggtttcctg gtgaatttct taaaagaaaa 360 atattttaag ttaagaaaaa aaaaaaaaa 389 43 279 DNA Homo sapien 43 actagtgaca agctcctggt cttgagatgt cttctcgtta aggagatggg ccttttggag 60 gtaaaggata aaatgaatga gttctgtcat gattcactat tctagaactt gcatgacctt 120 tactgtgtta gctctttgaa tgttcttgaa attttagact ttctttgtaa acaaataata 180 tgtccttatc attgtataaa agctgttatg tgcaacagtg tggagatcct tgtctgattt 240 aataaaatac ttaaacactg aaaaaaaaaa aaaaaaaaa 279 44 449 DNA Homo sapien misc_feature (1)...(449) n = A,T,C or G 44 actagtagca tcttttctac aacgttaaaa ttgcagaagt agcttatcat taaaaaacaa 60 caacaacaac aataacaata aatcctaagt gtaaatcagt tattctaccc cctaccaagg 120 atatcagcct gttttttccc ttttttctcc tgggaataat tgtgggcttc ttcccaaatt 180 tctacagcct ctttcctctt ctcatgcttg agcttccctg tttgcacgca tgcgttgtgc 240 aagantgggc tgtttngctt ggantncggt ccnagtggaa ncatgctttc ccttgttact 300 gttggaagaa actcaaacct tcnancccta ggtgttncca ttttgtcaag tcatcactgt 360 atttttgtac tggcattaac aaaaaaagaa atnaaatatt gttccattaa actttaataa 420 aactttaaaa gggaaaaaaa aaaaaaaaa 449 45 559 DNA Homo sapien misc_feature (1)...(559) n = A,T,C or G 45 actagtgtgg gggaatcacg gacacttaaa gtcaatctgc gaaataattc ttttattaca 60 cactcactga agtttttgag tcccagagag ccattctatg tcaaacattc caagtactct 120 ttgagagccc agcattacat caacatgccc gtgcagttca aaccgaagtc cgcaggcaaa 180 tttgaagctt tgcttgtcat tcaaacagat gaaggcaaga gtattgctat tcgactaatt 240 ggtgaagctc ttggaaaaaa ttnactagaa tactttttgt gttaagttaa ttacataagt 300 tgtattttgt taactttatc tttctacact acaattatgc ttttgtatat atattttgta 360 tgatggatat ctataattgt agattttgtt tttacaagct aatactgaag actcgactga 420 aatattatgt atctagccca tagtattgta cttaactttt acagggtgaa aaaaaaattc 480 tgtgtttgca ttgattatga tattctgaat aaatatggga atatatttta atgtgggtaa 540 aaaaaaaaaa aaaaaggaa 559 46 731 DNA Homo sapien misc_feature (1)...(731) n = A,T,C or G 46 actagttcta gtaccatggc tgtcatagat gcaaccatta tattccattt agtttcttcc 60 tcaggttccc taacaattgt ttgaaactga atatatatgt ttatgtatgt gtgtgtgttc 120 actgtcatgt atatggtgta tatgggatgt gtgcagtttt cagttatata tatattcata 180 tatacatatg catatatatg tataatatac atatatacat gcatacactt gtataatata 240 catatatata cacatatatg cacacatatn atcactgagt tccaaagtga gtctttattt 300 ggggcaattg tattctctcc ctctgtctgc tcactgggcc tttgcaagac atagcaattg 360 cttgatttcc tttggataag agtcttatct tcggcactct tgactctagc cttaacttta 420 gatttctatt ccagaatacc tctcatatct atcttaaaac ctaaganggg taaagangtc 480 ataagattgt agtatgaaag antttgctta gttaaattat atctcaggaa actcattcat 540 ctacaaatta aattgtaaaa tgatggtttg ttgtatctga aaaaatgttt agaacaagaa 600 atgtaactgg gtacctgtta tatcaaagaa cctcnattta ttaagtctcc tcatagccan 660 atccttatat ngccctctct gacctgantt aatananact tgaataatga atagttaatt 720 taggnttggg c 731 47 640 DNA Homo sapien misc_feature (1)...(640) n = A,T,C or G 47 tgcgngccgg tttggccctt ctttgtanga cactttcatc cgccctgaaa tcttcccgat 60 cgttaataac tcctcaggtc cctgcctgca cagggttttt tcttantttg ttgcctaaca 120 gtacaccaaa tgtgacatcc tttcaccaat atngattnct tcataccaca tcntcnatgg 180 anacgactnc aacaattttt tgatnacccn aaanactggg ggctnnaana agtacantct 240 ggagcagcat ggacctgtcn gcnactaang gaacaanagt nntgaacatt tacacaacct 300 ttggtatgtc ttactgaaag anagaaacat gcttctnncc ctagaccacg aggncaaccg 360 caganattgc caatgccaag tccgagcggt tagatcaggt aatacattcc atggatgcat 420 tacatacntt gtccccgaaa nanaagatgc cctaanggct tcttcanact ggtccngaaa 480 acanctacac ctggtgcttg ganaacanac tctttggaag atcatctggc acaagttccc 540 cccagtgggt tttnccttgg cacctanctt accanatcna ttcggaancc attctttgcc 600 ntggcnttnt nttgggacca ntcttctcac aactgnaccc 640 48 257 DNA Homo sapien 48 actagtatat gaaaatgtaa atatcacttg tgtactcaaa caaaagttgg tcttaagctt 60 ccaccttgag cagccttgga aacctaacct gcctctttta gcataatcac attttctaaa 120 tgattttctt tgttcctgaa aaagtgattt gtattagttt tacatttgtt ttttggaaga 180 ttatatttgt atatgtatca tcataaaata tttaaataaa aagtatcttt agagtgaaaa 240 aaaaaaaaaa aaaaaaa 257 49 652 DNA Homo sapien misc_feature (1)...(652) n = A,T,C or G 49 actagttcag atgagtggct gctgaagggg cccccttgtc attttcatta taacccaatt 60 tccacttatt tgaactctta agtcataaat gtataatgac ttatgaatta gcacagttaa 120 gttgacacta gaaactgccc atttctgtat tacactatca aataggaaac attggaaaga 180 tggggaaaaa aatcttattt taaaatggct tagaaagttt tcagattact ttgaaaattc 240 taaacttctt tctgtttcca aaacttgaaa atatgtagat ggactcatgc attaagactg 300 ttttcaaagc tttcctcaca tttttaaagt gtgattttcc ttttaatata catatttatt 360 ttctttaaag cagctatatc ccaacccatg actttggaga tatacctatn aaaccaatat 420 aacagcangg ttattgaagc agctttctca aatgttgctt cagatgtgca agttgcaaat 480 tttattgtat ttgtanaata caatttttgt tttaaactgt atttcaatct atttctccaa 540 gatgcttttc atatagagtg aaatatccca ngataactgc ttctgtgtcg tcgcatttga 600 cgcataactg cacaaatgaa cagtgtatac ctcttggttg tgcattnacc cc 652 50 650 DNA Homo sapien misc_feature (1)...(650) n = A,T,C or G 50 ttgcgctttg atttttttag ggcttgtgcc ctgtttcact tatagggtct agaatgcttg 60 tgttgagtaa aaaggagatg cccaatattc aaagctgcta aatgttctct ttgccataaa 120 gactccgtgt aactgtgtga acacttggga tttttctcct ctgtcccgag gtcgtcgtct 180 gctttctttt ttgggttctt tctagaagat tgagaaatgc atatgacagg ctgagancac 240 ctccccaaac acacaagctc tcagccacan gcagcttctc cacagcccca gcttcgcaca 300 ggctcctgga nggctgcctg ggggaggcag acatgggagt gccaaggtgg ccagatggtt 360 ccaggactac aatgtcttta tttttaactg tttgccactg ctgccctcac ccctgcccgg 420 ctctggagta ccgtctgccc canacaagtg ggantgaaat gggggtgggg gggaacactg 480 attcccantt agggggtgcc taactgaaca gtagggatan aaggtgtgaa cctgngaant 540 gcttttataa attatnttcc ttgttanatt tattttttaa tttaatctct gttnaactgc 600 ccngggaaaa ggggaaaaaa aaaaaaaaat tctntttaaa cacatgaaca 650 51 545 DNA Homo sapien misc_feature (1)...(545) n = A,T,C or G 51 tggcgtgcaa ccagggtagc tgaagtttgg gtctgggact ggagattggc cattaggcct 60 cctganattc cagctccctt ccaccaagcc cagtcttgct acgtggcaca gggcaaacct 120 gactcccttt gggcctcagt ttcccctccc cttcatgana tgaaaagaat actacttttt 180 cttgttggtc taacnttgct ggacncaaag tgtngtcatt attgttgtat tgggtgatgt 240 gtncaaaact gcagaagctc actgcctatg agaggaanta agagagatag tggatganag 300 ggacanaagg agtcattatt tggtatagat ccacccntcc caacctttct ctcctcagtc 360 cctgcncctc atgtntctgg tntggtgagt cctttgtgcc accanccatc atgctttgca 420 ttgctgccat cctgggaagg gggtgnatcg tctcacaact tgttgtcatc gtttganatg 480 catgctttct tnatnaaaca aanaaannaa tgtttgacag ngtttaaaat aaaaaanaaa 540 caaaa 545 52 678 DNA Homo sapien misc_feature (1)...(678) n = A,T,C or G 52 actagtagaa gaactttgcc gcttttgtgc ctctcacagg cgcctaaagt cattgccatg 60 ggaggaagac gatttggggg gggagggggg gggggcangg tccgtggggc tttccctant 120 ntatctccat ntccantgnn cnntgtcgcc tcttccctcg tcncattnga anttantccc 180 tggnccccnn nccctctccn ncctncncct cccccctccg ncncctccnn ctttttntan 240 ncttccccat ctccntcccc cctnanngtc ccaacnccgn cagcaatnnc ncacttnctc 300 nctccncncc tccnnccgtt cttctnttct cnacntntnc ncnnntnccn tgccnntnaa 360 annctctccc cnctgcaanc gattctctcc ctccncnnan ctntccactc cntncttctc 420 ncncgctcct nttcntcnnc ccacctctcn ccttcgnccc cantacnctc nccncccttn 480 cgnntcnttn nnntcctcnn accncccncc tcccttcncc cctcttctcc ccggtntntc 540 tctctcccnc nncncnncct cnncccntcc nngcgnccnt ttccgccccn cnccnccntt 600 ccttcntcnc cantccatcn cntntnccat nctncctncc nctcacnccc gctncccccn 660 ntctctttca cacngtcc 678 53 502 DNA Homo sapien misc_feature (1)...(502) n = A,T,C or G 53 tgaagatcct ggtgtcgcca tgggccgccg ccccgcccgt tgttaccggt attgtaagaa 60 caagccgtac ccaaagtctc gcttctgccg aggtgtccct gatgccaaaa ttcgcatttt 120 tgacctgggg cggaaaaang caaaantgga tgagtctccg ctttgtggcc acatggtgtc 180 agatcaatat gagcagctgt cctctgaagc cctgnangct gcccgaattt gtgccaataa 240 gtacatggta aaaagtngtg gcnaagatgc ttccatatcc gggtgcggnt ccaccccttc 300 cacgtcatcc gcatcaacaa gatgttgtcc tgtgctgggg ctgacaggct cccaacaggc 360 atgcgaagtg cctttggaaa acccanggca ctgtggccag ggttcacatt gggccaattn 420 atcatgttca tccgcaccaa ctgcagaaca angaacntgt naattnaagc cctgcccagg 480 gncaanttca aatttcccgg cc 502 54 494 DNA Homo sapien misc_feature (1)...(494) n = A,T,C or G 54 actagtccaa gaaaaatatg cttaatgtat attacaaagg ctttgtatat gttaacctgt 60 tttaatgcca aaagtttgct ttgtccacaa tttccttaag acctcttcag aaagggattt 120 gtttgcctta atgaatactg ttgggaaaaa acacagtata atgagtgaaa agggcagaag 180 caagaaattt ctacatctta gcgactccaa gaagaatgag tatccacatt tagatggcac 240 attatgagga ctttaatctt tccttaaaca caataatgtt ttcttttttc ttttattcac 300 atgatttcta agtatatttt tcatgcagga cagtttttca accttgatgt acagtgactg 360 tgttaaattt ttctttcagt ggcaacctct ataatcttta aaatatggtg agcatcttgt 420 ctgttttgaa ngggatatga cnatnaatct atcagatggg aaatcctgtt tccaagttag 480 aaaaaaaaaa aaaa 494 55 606 DNA Homo sapien misc_feature (1)...(606) n = A,T,C or G 55 actagtaaaa agcagcattg ccaaataatc cctaattttc cactaaaaat ataatgaaat 60 gatgttaagc tttttgaaaa gtttaggtta aacctactgt tgttagatta atgtatttgt 120 tgcttccctt tatctggaat gtggcattag cttttttatt ttaaccctct ttaattctta 180 ttcaattcca tgacttaagg ttggagagct aaacactggg atttttggat aacagactga 240 cagttttgca taattataat cggcattgta catagaaagg atatggctac cttttgttaa 300 atctgcactt tctaaatatc aaaaaaggga aatgaagtat aaatcaattt ttgtataatc 360 tgtttgaaac atgantttta tttgcttaat attanggctt tgcccttttc tgttagtctc 420 ttgggatcct gtgtaaaact gttctcatta aacaccaaac agttaagtcc attctctggt 480 actagctaca aattccgttt catattctac ntaacaattt aaattaactg aaatatttct 540 anatggtcta cttctgtcnt ataaaaacna aacttgantt nccaaaaaaa aaaaaaaaaa 600 aaaaaa 606 56 183 DNA Homo sapien 56 actagtatat ttaaacttac aggcttattt gtaatgtaaa ccaccatttt aatgtactgt 60 aattaacatg gttataatac gtacaatcct tccctcatcc catcacacaa ctttttttgt 120 gtgtgataaa ctgattttgg tttgcaataa aaccttgaaa aataaaaaaa aaaaaaaaaa 180 aaa 183 57 622 DNA Homo sapien misc_feature (1)...(622) n = A,T,C or G 57 actagtcact actgtcttct ccttgtagct aatcaatcaa tattcttccc ttgcctgtgg 60 gcagtggaga gtgctgctgg gtgtacgctg cacctgccca ctgagttggg gaaagaggat 120 aatcagtgag cactgttctg ctcagagctc ctgatctacc ccacccccta ggatccagga 180 ctgggtcaaa gctgcatgaa accaggccct ggcagcaacc tgggaatggc tggaggtggg 240 agagaacctg acttctcttt ccctctccct cctccaacat tactggaact ctatcctgtt 300 agggatcttc tgagcttgtt tccctgctgg gtgggacaga agacaaagga gaagggangg 360 tctacaanaa gcagcccttc tttgtcctct ggggttaatg agcttgacct ananttcatg 420 gaganaccan aagcctctga tttttaattt ccntnaaatg tttgaagtnt atatntacat 480 atatatattt ctttnaatnt ttgagtcttt gatatgtctt aaaatccant ccctctgccn 540 gaaacctgaa ttaaaaccat gaanaaaaat gtttncctta aagatgttan taattaattg 600 aaacttgaaa aaaaaaaaaa aa 622 58 433 DNA Homo sapien 58 gaacaaattc tgattggtta tgtaccgtca aaagacttga agaaatttca tgattttgca 60 gtgtggaagc gttgaaaatt gaaagttact gcttttccac ttgctcatat agtaaaggga 120 tcctttcagc tgccagtgtt gaataatgta tcatccagag tgatgttatc tgtgacagtc 180 accagcttta agctgaacca ttttatgaat accaaataaa tagacctctt gtactgaaaa 240 catatttgtg actttaatcg tgctgcttgg atagaaatat ttttactggt tcttctgaat 300 tgacagtaaa cctgtccatt atgaatggcc tactgttcta ttatttgttt tgacttgaat 360 ttatccacca aagacttcat ttgtgtatca tcaataaagt tgtatgtttc aactgaaaaa 420 aaaaaaaaaa aaa 433 59 649 DNA Homo sapien misc_feature (1)...(649) n = A,T,C or G 59 actagttatt atctgacttt cnggttataa tcattctaat gagtgtgaag tagcctctgg 60 tgtcatttgg atttgcattt ctctgatgag tgatgctatc aagcaccttt gctggtgctg 120 ttggccatat gtgtatgttc cctggagaag tgtctgtgct gagccttggc ccacttttta 180 attaggcgtn tgtcttttta ttactgagtt gtaaganttc tttatatatt ctggattcta 240 gacccttatc agatacatgg tttgcaaata ttttctccca ttctgtgggt tgtgttttca 300 ctttatcgat aatgtcctta gacatataat aaatttgtat tttaaaagtg acttgatttg 360 ggctgtgcaa ggtgggctca cgcttgtaat cccagcactt tgggagactg aggtgggtgg 420 atcatatgan gangctagga gttcgaggtc agcctggcca gcatagcgaa aacttgtctc 480 tacnaaaaat acaaaaatta gtcaggcatg gtggtgcacg tctgtaatac cagcttctca 540 ggangctgan gcacaaggat cacttgaacc ccagaangaa gangttgcag tganctgaag 600 atcatgccag ggcaacaaaa atgagaactt gtttaaaaaa aaaaaaaaa 649 60 423 DNA Homo sapien misc_feature (1)...(423) n = A,T,C or G 60 actagttcag gccttccagt tcactgacaa acatggggaa gtgtgcccag ctggctggaa 60 acctggcagt gataccatca agcctgatgt ccaaaagagc aaagaatatt tctccaagca 120 gaagtgagcg ctgggctgtt ttagtgccag gctgcggtgg gcagccatga gaacaaaacc 180 tcttctgtat tttttttttc cattagtana acacaagact cngattcagc cgaattgtgg 240 tgtcttacaa ggcagggctt tcctacaggg ggtgganaaa acagcctttc ttcctttggt 300 aggaatggcc tgagttggcg ttgtgggcag gctactggtt tgtatgatgt attagtagag 360 caacccatta atcttttgta gtttgtatna aacttganct gagaccttaa acaaaaaaaa 420 aaa 423 61 423 DNA Homo sapien misc_feature (1)...(423) n = A,T,C or G 61 cgggactgga atgtaaagtg aagttcggag ctctgagcac gggctcttcc cgccgggtcc 60 tccctcccca gaccccagag ggagaggccc accccgccca gccccgcccc agcccctgct 120 caggtctgag tatggctggg agtcgggggc cacaggcctc tagctgtgct gctcaagaag 180 actggatcag ggtanctaca agtggccggg ccttgccttt gggattctac cctgttccta 240 atttggtgtt ggggtgcggg gtccctggcc cccttttcca cactncctcc ctccngacag 300 caacctccct tggggcaatt gggcctggnt ctccncccgn tgttgcnacc ctttgttggt 360 ttaaggnctt taaaaatgtt annttttccc ntgccngggt taaaaaagga aaaaactnaa 420 aaa 423 62 683 DNA Homo sapien misc_feature (1)...(683) n = A,T,C or G 62 gctggagagg ggtacggact ttcttggagt tgtcccaggt tggaatgaga ctgaactcaa 60 gaagagaccc taagagactg gggaatggtt cctgccttca ggaaagtgaa agacgcttag 120 gctgtcaaca cttaaaggaa gtccccttga agcccagagt ggacagacta gacccattga 180 tggggccact ggccatggtc cgtggacaag acattccngt gggccatggc acaccggggg 240 ggatcaaaat gtgtacttgt ggggtctcgc cccttgccaa aaccaaacca ntcccactcc 300 tgtcnttgga ctttcttccc attccctcct ccccaaatgc acttcccctc ctccctctgc 360 ccctcctgtg tttttggaat tctgtttccc tcaaaattgt taatttttta nttttngacc 420 atgaacttat gtttggggtc nangttcccc ttnccaatgc atactaatat attaatggtt 480 atttattttt gaaatatttt ttaatgaact tggaaaaaat tnntggaatt tccttncttc 540 cnttttnttt ggggggggtg gggggntggg ttaaaatttt tttggaancc cnatnggaaa 600 ttnttacttg gggcccccct naaaaaantn anttccaatt cttnnatngc ccctnttccn 660 ctaaaaaaaa ananannaaa aan 683 63 731 DNA Homo sapien misc_feature (1)...(731) n = A,T,C or G 63 actagtcata aagggtgtgc gcgtcttcga cgtggcggtc ttggcgccac tgctgcgaga 60 cccggccctg gacctcaagg tcatccactt ggtgcgtgat ccccgcgcgg tggcgagttc 120 acggatccgc tcgcgccacg gcctcatccg tgagagccta caggtggtgc gcagccgaga 180 ccgcgagctc accgcatgcc cttcttggag gccgcgggcc acaagcttgg cgcccanaaa 240 gaaggcgtng ggggcccgca aantaccacg ctctgggcgc tatggaangt cctcttgcaa 300 taatattggt tnaaaanctg canaanagcc cctgcanccc cctgaactgg gntgcagggc 360 cncttacctn gtttggntgc ggttacaaag aacctgtttn ggaaaaccct nccnaaaacc 420 ttccgggaaa attntncaaa tttttnttgg ggaattnttg ggtaaacccc ccnaaaatgg 480 gaaacntttt tgccctnnaa antaaaccat tnggttccgg gggccccccc ncaaaaccct 540 tttttntttt tttntgcccc cantnncccc ccggggcccc tttttttngg ggaaaanccc 600 cccccctncc nanantttta aaagggnggg anaatttttn nttncccccc gggncccccn 660 ggngntaaaa nggtttcncc cccccgaggg gnggggnnnc ctcnnaaacc cntntcnnna 720 ccncnttttn n 731 64 313 DNA Homo sapien misc_feature (1)...(313) n = A,T,C or G 64 actagttgtg caaaccacga ctgaagaaag acgaaaagtg ggaaataact tgcaacgtct 60 gttagagatg gttgctacac atgttgggtc tgtagagaaa catcttgagg agcagattgc 120 taaagttgat agagaatatg aagaatgcat gtcagaagat ctctcggaaa atattaaaga 180 gattagagat aagtatgaga agaaagctac tctaattaag tcttctgaag aatgaagatn 240 aaatgttgat catgtatata tatccatagt gaataaaatt gtctcagtaa agttgtaaaa 300 aaaaaaaaaa aaa 313 65 420 DNA Homo sapien misc_feature (1)...(420) n = A,T,C or G 65 actagttccc tggcaggcaa gggcttccaa ctgaggcagt gcatgtgtgg cagagagagg 60 caggaagctg gcagtggcag cttctgtgtc tagggagggg tgtggctccc tccttccctg 120 tctgggaggt tggagggaag aatctaggcc ttagcttgcc ctcctgccac ccttcccctt 180 gtagatactg ccttaacact ccctcctctc tcagctgtgg ctgccaccca agccaggttt 240 ctccgtgctc actaatttat ttccaggaaa ggtgtgtgga agacatgagc cgtgtataat 300 atttgtttta acattttcat tgcaagtatt gaccatcatc cttggttgtg tatcgttgta 360 acacaaatta atgatattaa aaagcatcca aacaaagccn annnnnaana nnannngaaa 420 66 676 DNA Homo sapien misc_feature (1)...(676) n = A,T,C or G 66 actagtttcc tatgatcatt aaactcattc tcagggttaa gaaaggaatg taaatttctg 60 cctcaatttg tacttcatca ataagttttt gaagagtgca gatttttagt caggtcttaa 120 aaataaactc acaaatctgg atgcatttct aaattctgca aatgtttcct ggggtgactt 180 aacaaggaat aatcccacaa tatacctagc tacctaatac atggagctgg ggctcaaccc 240 actgttttta aggatttgcg cttacttgtg gctgaggaaa aataagtagt tccgagggaa 300 gtagttttta aatgtgagct tatagatngg aaacagaata tcaacttaat tatggaaatt 360 gttagaaacc tgttctcttg ttatctgaat cttgattgca attactattg tactggatag 420 actccagccc attgcaaagt ctcagatatc ttanctgtgt agttgaattc cttggaaatt 480 ctttttaaga aaaaattgga gtttnaaaga aataaacccc tttgttaaat gaagcttggc 540 tttttggtga aaaanaatca tcccgcaggg cttattgttt aaaaanggaa ttttaagcct 600 ccctggaaaa anttgttaat taaatgggga aaatgntggg naaaaattat ccgttagggt 660 ttaaagggaa aactta 676 67 620 DNA Homo sapien misc_feature (1)...(620) n = A,T,C or G 67 caccattaaa gctgcttacc aagaacttcc ccagcatttt gacttccttg tttgatagct 60 gaattgtgag caggtgatag aagagccttt ctagttgaac atacagataa tttgctgaat 120 acattccatt taatgaaggg gttacatctg ttacgaagct actaagaagg agcaagagca 180 taggggaaaa aaatctgatc agaacgcatc aaactcacat gtgccccctc tactacaaac 240 agattgtagt gctgtggtgg tttattccgt tgtgcagaac ttgcaagctg agtcactaaa 300 cccaaagaga ggaaattata ggttagttaa acattgtaat cccaggaact aagtttaatt 360 cacttttgaa gtgttttgtt ttttattttt ggtttgtctg atttactttg ggggaaaang 420 ctaaaaaaaa agggatatca atctctaatt cagtgcccac taaaagttgt ccctaaaaag 480 tctttactgg aanttatggg actttttaag ctccaggtnt tttggtcctc caaattaacc 540 ttgcatgggc cccttaaaat tgttgaangg cattcctgcc tctaagtttg gggaaaattc 600 ccccnttttn aaaatttgga 620 68 551 DNA Homo sapien misc_feature (1)...(551) n = A,T,C or G 68 actagtagct ggtacataat cactgaggag ctatttctta acatgctttt atagaccatg 60 ctaatgctag accagtattt aagggctaat ctcacacctc cttagctgta agagtctggc 120 ttagaacaga cctctctgtg caataacttg tggccactgg aaatccctgg gccggcattt 180 gtattggggt tgcaatgact cccaagggcc aaaagagtta aaggcacgac tgggatttct 240 tctgagactg tggtgaaact ccttccaagg ctgagggggt cagtangtgc tctgggaggg 300 actcggcacc actttgatat tcaacaagcc acttgaagcc caattataaa attgttattt 360 tacagctgat ggaactcaat ttgaaccttc aaaactttgt tagtttatcc tattatattg 420 ttaaacctaa ttacatttgt ctagcattgg atttggttcc tgtngcatat gtttttttcn 480 cctatgtgct cccctccccc nnatcttaat ttaaaccnca attttgcnat tcnccnnnnn 540 nannnannna a 551 69 396 DNA Homo sapien misc_feature (1)...(396) n = A,T,C or G 69 cagaaatgga aagcagagtt ttcatttctg tttataaacg tctccaaaca aaaatggaaa 60 gcagagtttt cattaaatcc ttttaccttt tttttttctt ggtaatcccc tcaaataaca 120 gtatgtggga tattgaatgt taaagggata tttttttcta ttatttttat aattgtacaa 180 aattaagcaa atgttaaaag ttttatatgc tttattaatg ttttcaaaag gtatnataca 240 tgtgatacat tttttaagct tcagttgctt gtcttctggt actttctgtt atgggctttt 300 ggggagccan aaaccaatct acnatctctt tttgtttgcc aggacatgca ataaaattta 360 aaaaataaat aaaaactatt nagaaattga aaaaaa 396 70 536 DNA Homo sapien misc_feature (1)...(536) n = A,T,C or G 70 actagtgcaa aagcaaatat aaacatcgaa aaggcgttcc tcacgttagc tgaagatatc 60 cttcgaaaga cccctgtaaa agagcccaac agtgaaaatg tagatatcag cagtggagga 120 ggcgtgacag gctggaagag caaatgctgc tgagcattct cctgttccat cagttgccat 180 ccactacccc gttttctctt cttgctgcaa aataaaccac tctgtccatt tttaactcta 240 aacagatatt tttgtttctc atcttaacta tccaagccac ctattttatt tgttctttca 300 tctgtgactg cttgctgact ttatcataat tttcttcaaa caaaaaaatg tatagaaaaa 360 tcatgtctgt gacttcattt ttaaatgnta cttgctcagc tcaactgcat ttcagttgtt 420 ttatagtcca gttcttatca acattnaaac ctatngcaat catttcaaat ctattctgca 480 aattgtataa gaataaaagt tagaatttaa caattaaaaa aaaaaaaaaa aaaaaa 536 71 865 DNA Homo sapien misc_feature (1)...(865) n = A,T,C or G 71 gacaaagcgt taggagaaga anagaggcag ggaanactnc ccaggcacga tggccncctt 60 cccaccagca accagcgccc cccaccagcc cccaggcccg gacgacgaag actccatcct 120 ggattaatct nacctctntc gcctgnccca ttcctacctc ggaggtggag gccggaaagg 180 tcncaccaag aganaanctg ctgccaacac caaccgcccc agccctggcg ggcacganag 240 gaaactggtg accaatctgc agaattctna gaggaanaag cnaggggccc cgcgctnaga 300 cagagctgga tatgangcca gaccatggac nctacncccn ncaatncana cgggactgcg 360 gaagatggan gacccncgac nngatcaggc cngctnncca nccccccacc cctatgaatt 420 attcccgctg aangaatctc tgannggctt ccannaaagc gcctccccnc cnaacgnaan 480 tncaacatng ggattanang ctgggaactg naaggggcaa ancctnnaat atccccagaa 540 acaanctctc ccnaanaaac tggggcncct catnggtggn accaactatt aactaaaccg 600 cacgccaagn aantataaaa ggggggcccc tccncggnng accccctttt gtcccttaat 660 ganggttatc cnccttgcgt accatggtnc ccnnttctgt ntgnatgttt ccnctcccct 720 ccncctatnt cnagccgaac tcnnatttnc ccgggggtgc natcnantng tncncctttn 780 ttngttgncc cngccctttc cgncggaacn cgtttccccg ttantaacgg cacccggggn 840 aagggtgntt ggccccctcc ctccc 865 72 560 DNA Homo sapien misc_feature (1)...(560) n = A,T,C or G 72 cctggacttg tcttggttcc agaacctgac gacccggcga cggcgacgtc tcttttgact 60 aaaagacagt gtccagtgct ccngcctagg agtctacggg gaccgcctcc cgcgccgcca 120 ccatgcccaa cttctctggc aactggaaaa tcatccgatc ggaaaacttc gangaattgc 180 tcnaantgct gggggtgaat gtgatgctna ngaanattgc tgtggctgca gcgtccaagc 240 cagcagtgga gatcnaacag gagggagaca ctttctacat caaaacctcc accaccgtgc 300 gcaccacaaa gattaacttc nnngttgggg aggantttga ggancaaact gtggatngga 360 ngcctgtnaa aacctggtga aatgggagaa tganaataaa atggtctgtg ancanaaact 420 cctgaaagga gaaggccccc anaactcctg gaccngaaaa actgacccnc cnatngggga 480 actgatnctt gaaccctgaa cgggcgggat ganccttttt tnttgccncc naangggttc 540 tttccntttc cccaaaaaaa 560 73 379 DNA Homo sapien misc_feature (1)...(379) n = A,T,C or G 73 ctggggancc ggcggtnngc nccatntcnn gncgcgaagg tggcaataaa aanccnctga 60 aaccgcncaa naaacatgcc naagatatgg acgaggaaga tngngctttc nngnacaanc 120 gnanngagga acanaacaaa ctcnangagc tctcaagcta atgccgcggg gaaggggccc 180 ttggccacnn gtggaattaa gaaatctggc aaanngtann tgttccttgt gcctnangag 240 ataagngacc ctttatttca tctgtattta aacctctctn ttccctgnca taacttcttt 300 tnccacgtan agntggaant anttgttgtc ttggactgtt gtncatttta gannaaactt 360 ttgttcaaaa aaaaaataa 379 74 437 DNA Homo sapien misc_feature (1)...(437) n = A,T,C or G 74 actagttcag actgccacgc caaccccaga aaatacccca catgccagaa aagtgaagtc 60 ctaggtgttt ccatctatgt ttcaatctgt ccatctacca ggcctcgcga taaaaacaaa 120 acaaaaaaac gctgccaggt tttanaagca gttctggtct caaaaccatc aggatcctgc 180 caccagggtt cttttgaaat agtaccacat gtaaaaggga atttggcttt cacttcatct 240 aatcactgaa ttgtcaggct ttgattgata attgtagaaa taagtagcct tctgttgtgg 300 gaataagtta taatcagtat tcatctcttt gttttttgtc actcttttct ctctnattgt 360 gtcatttgta ctgtttgaaa aatatttctt ctataaaatt aaactaacct gccttaaaaa 420 aaaaaaaaaa aaaaaaa 437 75 579 DNA Homo sapien misc_feature (1)...(579) n = A,T,C or G 75 ctccgtcgcc gccaagatga tgtgcggggc gccctccgcc acgcagccgg ccaccgccga 60 gacccagcac atcgccgacc aggtgaggtc ccagcttgaa gagaaagaaa acaagaagtt 120 ccctgtgttt aaggccgtgt cattcaagag ccaggtggtc gcggggacaa actacttcat 180 caaggtgcac gtcggcgacg aggacttcgt acacctgcga gtgttccaat ctctccctca 240 tgaaaacaag cccttgacct tatctaacta ccagaccaac aaagccaagc atgatgagct 300 gacctatttc tgatcctgac tttggacaag gcccttcagc cagaagactg acaaagtcat 360 cctccgtcta ccagagcgtg cacttgtgat cctaaaataa gcttcatctc cgggctgtgc 420 ccttggggtg gaaggggcan gatctgcact gcttttgcat ttctcttcct aaatttcatt 480 gtgttgattc tttccttcca ataggtgatc ttnattactt tcagaatatt ttccaaatna 540 gatatatttt naaaatcctt aaaaaaaaaa aaaaaaaaa 579 76 666 DNA Homo sapien misc_feature (1)...(666) n = A,T,C or G 76 gtttatccta tctctccaac cagattgtca gctccttgag ggcaagagcc acagtatatt 60 tccctgtttc ttccacagtg cctaataata ctgtggaact aggttttaat aattttttaa 120 ttgatgttgt tatgggcagg atggcaacca gaccattgtc tcagagcagg tgctggctct 180 ttcctggcta ctccatgttg gctagcctct ggtaacctct tacttattat cttcaggaca 240 ctcactacag ggaccaggga tgatgcaaca tccttgtctt tttatgacag gatgtttgct 300 cagcttctcc aacaataaaa agcacgtggt aaaacacttg cggatattct ggactgtttt 360 taaaaaatat acagtttacc gaaaatcata ttatcttaca atgaaaagga ntttatagat 420 cagccagtga acaacctttt cccaccatac aaaaattcct tttcccgaan gaaaanggct 480 ttctcaataa ncctcacttt cttaanatct tacaagatag ccccganatc ttatcgaaac 540 tcattttagg caaatatgan ttttattgtn cgttacttgt ttcaaaattt ggtattgtga 600 atatcaatta ccacccccat ctcccatgaa anaaanggga aanggtgaan ttcntaancg 660 cttaaa 666 77 396 DNA Homo sapien misc_feature (1)...(396) n = A,T,C or G 77 ctgcagcccg ggggatccac taatctacca nggttatttg gcagctaatt ctanatttgg 60 atcattgccc aaagttgcac ttgctggtct cttgggattt ggccttggaa aggtatcata 120 catanganta tgccanaata aattccattt ttttgaaaat canctccntg gggctggttt 180 tggtccacag cataacangc actgcctcct tacctgtgag gaatgcaaaa taaagcatgg 240 attaagtgag aagggagact ctcagccttc agcttcctaa attctgtgtc tgtgactttc 300 gaagtttttt aaacctctga atttgtacac atttaaaatt tcaagtgtac tttaaaataa 360 aatacttcta atgggaacaa aaaaaaaaaa aaaaaa 396 78 793 DNA Homo sapien misc_feature (1)...(793) n = A,T,C or G 78 gcatcctagc cgccgactca cacaaggcag gtgggtgagg aaatccagag ttgccatgga 60 gaaaattcca gtgtcagcat tcttgctcct tgtggccctc tcctacactc tggccagaga 120 taccacagtc aaacctggag ccaaaaagga cacaaaggac tctcgaccca aactgcccca 180 gaccctctcc agaggttggg gtgaccaact catctggact cagacatatg aagaagctct 240 atataaatcc aagacaagca acaaaccctt gatgattatt catcacttgg atgagtgccc 300 acacagtcna gctttaaaga aagtgtttgc tgaaaataaa gaaatccaga aattggcaga 360 gcagtttgtc ctcctcaatc tggtttatga aacaactgac aaacaccttt ctcctgatgg 420 ccagtatgtc ccaggattat gtttgttgac ccatctctga cagttgaagc cgatatcctg 480 ggaagatatt cnaaccgtct ctatgcttac aaactgcaga tacgctctgt tgcttgacac 540 atgaaaaagc tctcaagttg ctnaaaatga attgtaagaa aaaaaatctc cagccttctg 600 tctgtcggct tgaaaattga aaccagaaaa atgtgaaaaa tggctattgt ggaacanatn 660 gacacctgat taggttttgg ttatgttcac cactattttt aanaaaanan nttttaaaat 720 ttggttcaat tntctttttn aaacaatntg tttctacntt gnganctgat ttctaaaaaa 780 aataatnttt ggc 793 79 456 DNA Homo sapien misc_feature (1)...(456) n = A,T,C or G 79 actagtatgg ggtgggaggc cccacccttc tcccctaggc gctgttcttg ctccaaaggg 60 ctccgtggag agggactggc agagctgang ccacctgggg ctggggatcc cactcttctt 120 gcagctgttg agcgcaccta accactggtc atgcccccac ccctgctctc cgcacccgct 180 tcctcccgac cccangacca ggctacttct cccctcctct tgcctccctc ctgcccctgc 240 tgcctctgat cgtangaatt gangantgtc ccgccttgtg gctganaatg gacagtggca 300 ggggctggaa atgggtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gcnccccccc 360 tgcaagaccg agattgaggg aaancatgtc tgctgggtgt gaccatgttt cctctccata 420 aantncccct gtgacnctca naaaaaaaaa aaaaaa 456 80 284 DNA Homo sapien misc_feature (1)...(284) n = A,T,C or G 80 ctttgtacct ctagaaaaga taggtattgt gtcatgaaac ttgagtttaa attttatata 60 taaaactaaa agtaatgctc actttagcaa cacatactaa aattggaacc atactgagaa 120 gaatagcatg acctccgtgc aaacaggaca agcaaatttg tgatgtgttg attaaaaaga 180 aataaataaa tgtgtatatg tgtaacttgt atgtttatgt ggaatacaga ttgggaaata 240 aaatgtattt cttactgtga aaaaaaaaaa aaaaaaaaaa aana 284 81 671 DNA Homo sapien misc_feature (1)...(671) n = A,T,C or G 81 gccaccaaca ttccaagcta ccctgggtac ctttgtgcag tagaagctag tgagcatgtg 60 agcaagcggt gtgcacacgg agactcatcg ttataattta ctatctgcca agagtagaaa 120 gaaaggctgg ggatatttgg gttggcttgg ttttgatttt ttgcttgttt gtttgttttg 180 tactaaaaca gtattatctt ttgaatatcg tagggacata agtatataca tgttatccaa 240 tcaagatggc tagaatggtg cctttctgag tgtctaaaac ttgacacccc tggtaaatct 300 ttcaacacac ttccactgcc tgcgtaatga agttttgatt catttttaac cactggaatt 360 tttcaatgcc gtcattttca gttagatnat tttgcacttt gagattaaaa tgccatgtct 420 atttgattag tcttattttt ttatttttac aggcttatca gtctcactgt tggctgtcat 480 tgtgacaaag tcaaataaac ccccnaggac aacacacagt atgggatcac atattgtttg 540 acattaagct ttggccaaaa aatgttgcat gtgttttacc tcgacttgct aaatcaatan 600 canaaaggct ggctnataat gttggtggtg aaataattaa tnantaacca aaaaaaaaan 660 aaaaaaaaaa a 671 82 217 DNA Homo sapien misc_feature (1)...(217) n = A,T,C or G 82 ctgcagatgt ttcttgaatg ctttgtcaaa ttaanaaagt taaagtgcaa taatgtttga 60 agacaataag tggtggtgta tcttgtttct aataagataa acttttttgt ctttgcttta 120 tcttattagg gagttgtatg tcagtgtata aaacatactg tgtggtataa caggcttaat 180 aaattcttta aaaggaaaaa aaaaaaaaaa aaaaaaa 217 83 460 DNA Homo sapien misc_feature (1)...(460) n = A,T,C or G 83 cgcgagtggg agcaccagga tctcgggctc ggaacgagac tgcacggatt gttttaagaa 60 aatggcagac aaaccagaca tgggggaaat cgccagcttc gatnaggcca agctgaanaa 120 aacggagacg caggagaaga acaccctgcc gaccaaagag accattgagc angagaagcg 180 gagtgaaatt tcctaagatc ctggaggatt tcctaccccc gtcctcttcg agaccccagt 240 cgtgatgtgg aggaagagcc acctgcaaga tggacacgag ccacaagctg cactgtgaac 300 ctgggcactc cgcgccgatg ccaccggcct gtgggtctct gaagggaccc cccccaatcg 360 gactgccaaa ttctccggtt tgccccggga tattatacaa nattatttgt atgaataatg 420 annataaaac acacctcgtg gcancaaana aaaaaaaaaa 460 84 323 DNA Homo sapien misc_feature (1)...(323) n = A,T,C or G 84 tggtggatct tggctctgtg gagctgctgg gacgggatct aaaagactat tctggaagct 60 gtggtccaan gcattttgct ggcttaacgg gtcccggaac aaaggacacc agctctctaa 120 aattgaagtt tacccganat aacaatcttt tgggcagaga tgcctatttt aacaaacncc 180 gtccctgcgc aacaacnaac aatctctggg aaataccggc catgaacntg ctgtctcaat 240 cnancatctc tctagctgac cgatcatatc gtcccagatt actacanatc ataataattg 300 atttcctgta naaaaaaaaa aaa 323 85 771 DNA Homo sapien misc_feature (1)...(771) n = A,T,C or G 85 aaactgggta ctcaacactg agcagatctg ttctttgagc taaaaaccat gtgctgtacc 60 aanagtttgc tcctggctgc tttgatgtca gtgctgctac tccacctctg cggcgaatca 120 gaagcaagca actttgactg ctgtcttgga tacacagacc gtattcttca tcctaaattt 180 attgtgggct tcacacggca gctggccaat gaaggctgtg acatcaatgc tatcatcttt 240 cacacaaaga aaaagttgtc tgtgtgcgca aatccaaaac agacttgggt gaaatatatt 300 gtgcgtctcc tcagtaaaaa agtcaagaac atgtaaaaac tgtggctttt ctggaatgga 360 attggacata gcccaagaac agaaagaact tgctggggtt ggaggtttca cttgcacatc 420 atgganggtt tagtgcttat cttatttgtg cctcctggac ttgtccaatt natgaagtta 480 atcatattgc atcatanttt gctttgttta acatcacatt naaattaaac tgtattttat 540 gttatttata gctntaggtt ttctgtgttt aactttttat acnaantttc ctaaactatt 600 ttggtntant gcaanttaaa aattatattt ggggggggaa taaatattgg antttctgca 660 gccacaagct ttttttaaaa aaccantaca nccnngttaa atggtnggtc ccnaatggtt 720 tttgcttttn antagaaaat ttnttagaac natttgaaaa aaaaaaaaaa a 771 86 628 DNA Homo sapien misc_feature (1)...(628) n = A,T,C or G 86 actagtttgc tttacatttt tgaaaagtat tatttttgtc caagtgctta tcaactaaac 60 cttgtgttag gtaagaatgg aatttattaa gtgaatcagt gtgacccttc ttgtcataag 120 attatcttaa agctgaagcc aaaatatgct tcaaaagaaa angactttat tgttcattgt 180 agttcataca ttcaaagcat ctgaactgta gtttctatag caagccaatt acatccataa 240 gtggagaang aaatagatta atgtcnaagt atgattggtg gagggagcaa ggttgaagat 300 aatctggggt tgaaattttc tagttttcat tctgtacatt tttagttnga catcagattt 360 gaaatattaa tgtttacctt tcaatgtgtg gtatcagctg gactcantaa cacccctttc 420 ttccctnggg gatggggaat ggattattgg aaaatggaaa gaaaaaagta cttaaagcct 480 tcctttcnca gtttctggct cctaccctac tgatttancc agaataagaa aacattttat 540 catcntctgc tttattccca ttaatnaant tttgatgaat aaatctgctt ttatgcnnac 600 ccaaggaatt nagtggnttc ntcnttgt 628 87 518 DNA Homo sapien misc_feature (1)...(518) n = A,T,C or G 87 ttttttattt tttttagaga gtagttcagc ttttatttat aaatttattg cctgttttat 60 tataacaaca ttatactgtt tatggtttaa tacatatggt tcaaaatgta taatacatca 120 agtagtacag ttttaaaatt ttatgcttaa aacaagtttt gtgtaaaaaa tgcagataca 180 ttttacatgg caaatcaatt tttaagtcat cctaaaaatt gatttttttt tgaaatttaa 240 aaacacattt aatttcaatt tctctcttat ataaccttta ttactatagc atggtttcca 300 ctacagttta acaatgcagc aaaattccca tttcacggta aattgggttt taagcggcaa 360 ggttaaaatg ctttgaggat cctnaatacc ctttgaactt caaatgaagg ttatggttgt 420 naatttaacc ctcatgccat aagcagaagc acaagtttag ctgcattttg ctctaaactg 480 taaaancgag ccccccgttg aaaaagcaaa agggaccc 518 88 1844 DNA Homo sapien 88 gagacagtga atcctagtat caaaggattt ttggcctcag aaaaagttgt tgattatttt 60 tattttattt tatttttcga gactccgtct caaaaaaaaa aaaaaaaaaa agaatcacaa 120 ggtatttgct aaagcatttt gagctgcttg gaaaaaggga agtagttgca gtagagtttc 180 ttccatcttc ttggtgctgg gaagccatat atgtgtcttt tactcaagct aaggggtata 240 agcttatgtg ttgaatttgc tacatctata tttcacatat tctcacaata agagaatttt 300 gaaatagaaa tatcatagaa catttaagaa agtttagtat aaataatatt ttgtgtgttt 360 taatcccttt gaagggatct atccaaagaa aatattttac actgagctcc ttcctacacg 420 tctcagtaac agatcctgtg ttagtctttg aaaatagctc attttttaaa tgtcagtgag 480 tagatgtagc atacatatga tgtataatga cgtgtattat gttaacaatg tctgcagatt 540 ttgtaggaat acaaaacatg gcctttttta taagcaaaac gggccaatga ctagaataac 600 acatagggca atctgtgaat atgtattata agcagcattc cagaaaagta gttggtgaaa 660 taattttcaa gtcaaaaagg gatatggaaa gggaattatg agtaacctct attttttaag 720 ccttgctttt aaattaaacg ctacagccat ttaagccttg aggataataa agcttgagag 780 taataatgtt aggttagcaa aggtttagat gtatcacttc atgcatgcta ccatgatagt 840 aatgcagctc ttcgagtcat ttctggtcat tcaagatatt cacccttttg cccatagaaa 900 gcaccctacc tcacctgctt actgacattg tcttagctga tcacaagatc attatcagcc 960 tccattattc cttactgtat ataaaataca gagttttata ttttcctttc ttcgtttttc 1020 accatattca aaacctaaat ttgtttttgc agatggaatg caaagtaatc aagtgttcgt 1080 gctttcacct agaagggtgt ggtcctgaag gaaagaggtc cctaaatatc ccccaccctg 1140 ggtgctcctc cttccctggt accctgacta ccagaagtca ggtgctagag cagctggaga 1200 agtgcagcag cctgtgcttc cacagatggg ggtgctgctg caacaaggct ttcaatgtgc 1260 ccatcttagg gggagaagct agatcctgtg cagcagcctg gtaagtcctg aggaggttcc 1320 attgctcttc ctgctgctgt cctttgcttc tcaacggggc tcgctctaca gtctagagca 1380 catgcagcta acttgtgcct ctgcttatgc atgagggtta aattaacaac cataaccttc 1440 atttgaagtt caaaggtgta ttcaggatcc tcaaagcatt ttaaccttgc cgcttaaaac 1500 ccaatttacc gtgaaatggg aattttgctg cattgttaaa ctgtagtgga aaccatgcta 1560 tagtaataaa ggttatataa gagagaaatt gaaattaaat gtgtttttaa atttcaaaaa 1620 aaaatcaatc tttaggatga cttaaaaatt gatttgccat gtaaaatgta tctgcatttt 1680 ttacacaaaa cttgttttaa gcataaaatt ttaaaactgt actacttgat gtattataca 1740 ttttgaacca tatgtattaa accataaaca gtataatgtt gttataataa aacaggcaat 1800 aaatttataa ataaaagctg aaaaaaaaaa aaaaaaaaaa aaaa 1844 89 523 DNA Homo sapien misc_feature (1)...(523) n = A,T,C or G 89 tttttttttt tttttttagt caatccacat ttattgatca cttattatgt accaggcact 60 gggataaaga tgactgttag tcactcacag taaggaagaa aactagcaaa taagacgatt 120 acaatatgat gtagaaaatg ctaagccaga gatatagaaa ggtcctattg ggtccttctg 180 tcaccttgtc tttccacatc cctacccttc acaggccttc cctccagctt cctgcccccg 240 ctccccactg cagatcccct gggattttgc ctagagctaa acgagganat gggccccctg 300 gccctggcat gacttgaacc caaccacaga ctgggaaagg gagcctttcg anagtggatc 360 actttgatna gaaaacacat agggaattga agagaaantc cccaaatggc cacccgtgct 420 ggtgctcaag aaaagtttgc agaatggata aatgaaggat caagggaatt aatanatgaa 480 taattgaatg gtggctcaat aagaatgact ncnttgaatg acc 523 90 604 DNA Homo sapien misc_feature (1)...(604) n = A,T,C or G 90 ccagtgtggt ggaatgcaaa gattaccccg gaagctttcg agaagctggg attccctgca 60 gcaaaggaaa tagccaatat gtgtcgtttc tatgaaatga agccagaccg agatgtcaat 120 ctcacccacc aactaaatcc caaagtcaaa agcttcagcc agtttatctc agagaaccag 180 gggagccttc aagggcatgt agaaaatcag ctgttcagat aggcctctgc accacacagc 240 ctctttcctc tctgatcctt ttcctcttta cggcacaaca ttcatgtttg acagaacatg 300 ctggaatgca attgtttgca acaccgaagg atttcctgcg gtcgcctctt cagtaggaag 360 cactgcattg gtgataggac acggtaattt gattcacatt taacttgcta gttagtgata 420 aggggtggta cacctgtttg gtaaaatgag aagcctcgga aacttgggag cttctctcct 480 accactaatg gggagggcag attattactg ggatttctcc tggggtgaat taatttcaag 540 ccctaattgc tgaaattccc ctnggcaggc tccagttttc tcaactgcat tgcaaaattc 600 cccc 604 91 858 DNA Homo sapien misc_feature (1)...(858) n = A,T,C or G 91 tttttttttt ttttttttta tgattattat tttttttatt gatctttaca tcctcagtgt 60 tggcagagtt tctgatgctt aataaacatt tgttctgatc agataagtgg aaaaaattgt 120 catttcctta ttcaagccat gcttttctgt gatattctga tcctagttga acatacagaa 180 ataaatgtct aaaacagcac ctcgattctc gtctataaca ggactaagtt cactgtgatc 240 ttaaataagc ttggctaaaa tgggacatga gtggaggtag tcacacttca gcgaagaaag 300 agaatctcct gtataatctc accaggagat tcaacgaatt ccaccacact ggactagtgg 360 atcccccggg ctgcaggaat tcgatatcaa gcttatcgat accgtcgacc tcgagggggg 420 gcccggtacc caattcgccc tatagtgagt cgtattacgc gcgctcactg gccgtcgttt 480 tacaacgtcg tgactgggaa aaccctggcg ttacccaact taatcgcctt gcagcacatc 540 cccctttcgc cagctggcgt aatagcgaan agcccgcacc gatcgccctt ncaacagttg 600 cgcagcctga atggcgaatg ggacgcgccc tgtagcggcg cattaaagcg cggcngggtg 660 tggnggntcc cccacgtgac cgntacactt ggcagcgcct tacgccggtc nttcgctttc 720 ttcccttcct ttctcgcacc gttcgccggg tttccccgnn agctnttaat cgggggnctc 780 cctttanggg tncnaattaa nggnttacng gaccttngan cccaaaaact ttgattaggg 840 ggaaggtccc cgaagggg 858 92 585 DNA Homo sapien misc_feature (1)...(585) n = A,T,C or G 92 gttgaatctc ctggtgagat tatacaggag attctctttc ttcgctgaag tgtgactacc 60 tccactcatg tcccatttta gccaagctta tttaagatca cagtgaactt agtcctgtta 120 tagacgagaa tcgaggtgct gttttagaca tttatttctg tatgttcaac taggatcaga 180 atatcacaga aaagcatggc ttgaataagg aaatgacaat tttttccact tatctgatca 240 gaacaaatgt ttattaagca tcagaaactc tgccaacact gaggatgtaa agatcaataa 300 aaaaaataat aatcatnann naaanannan nngaagggcg gccgccaccg cggtggagct 360 ccagcttttg ttccctttag tgagggttaa ttgcgcgctt ggcgttaatc atggtcatag 420 ctgtttcctg tgtgaaattg ttatccggct cacaattccn cncaacatac gagccgggaa 480 gcntnangtg taaaagcctg ggggtgccta attgagtgag ctnactcaca ttaattgngt 540 tgcgctccac ttgcccgctt ttccantccg ggaaacctgt tcgnc 585 93 567 DNA Homo sapien misc_feature (1)...(567) n = A,T,C or G 93 cggcagtgtt gctgtctgcg tgtccacctt ggaatctggc tgaactggct gggaggacca 60 agactgcggc tggggtgggc anggaaggga accgggggct gctgtgaagg atcttggaac 120 ttccctgtac ccaccttccc cttgcttcat gtttgtanag gaaccttgtg ccggccaagc 180 ccagtttcct tgtgtgatac actaatgtat ttgctttttt tgggaaatan anaaaaatca 240 attaaattgc tantgtttct ttgaannnnn nnnnnnnnnn nnnnnnnggg ggggncgccc 300 ccncggngga aacnccccct tttgttccct ttaattgaaa ggttaattng cncncntggc 360 gttaanccnt gggccaaanc tngttncccg tgntgaaatt gttnatcccc tcccaaattc 420 ccccccnncc ttccaaaccc ggaaancctn annntgttna ancccggggg gttgcctaan 480 ngnaattnaa ccnaaccccc ntttaaatng nntttgcncn ccacnngccc cnctttccca 540 nttcggggaa aaccctntcc gtgccca 567 94 620 DNA Homo sapien misc_feature (1)...(620) n = A,T,C or G 94 actagtcaaa aatgctaaaa taatttggga gaaaatattt tttaagtagt gttatagttt 60 catgtttatc ttttattatg ttttgtgaag ttgtgtcttt tcactaatta cctatactat 120 gccaatattt ccttatatct atccataaca tttatactac atttgtaana naatatgcac 180 gtgaaactta acactttata aggtaaaaat gaggtttcca anatttaata atctgatcaa 240 gttcttgtta tttccaaata gaatggactt ggtctgttaa gggctaagga gaagaggaag 300 ataaggttaa aagttgttaa tgaccaaaca ttctaaaaga aatgcaaaaa aaaagtttat 360 tttcaagcct tcgaactatt taaggaaagc aaaatcattt cctaaatgca tatcatttgt 420 gagaatttct cattaatatc ctgaatcatt catttcacta aggctcatgt tnactccgat 480 atgtctctaa gaaagtacta tttcatggtc caaacctggt tgccatantt gggtaaaggc 540 tttcccttaa gtgtgaaant atttaaaatg aaattttcct ctttttaaaa attctttana 600 agggttaagg gtgttgggga 620 95 470 DNA Homo sapien misc_feature (1)...(470) n = A,T,C or G 95 ctcgaccttc tctgcacagc ggatgaaccc tgagcagctg aagaccagaa aagccactat 60 nactttntgc ttaattcang agcttacang attcttcaaa gagtgngtcc agcatccttt 120 gaaacatgag ttcttaccag cagaagcaga cctttacccc accacctcag cttcaacagc 180 agcaggtgaa acaacccatc cagcctccac ctnaggaaat atttgttccc acaaccaagg 240 agccatgcca ctcaaaggtt ccacaacctg naaacacaaa nattccagag ccaggctgta 300 ccaaggtccc tgagccaggg ctgtaccaan gtccctgagc caggttgtac caangtccct 360 gagccaggat gtaccaaggt ccctgancca ggttgtccaa ggtccctgag ccaggctaca 420 ccaagggcct gngccaggca gcatcaangt ccctgaccaa ggcttatcaa 470 96 660 DNA Homo sapien misc_feature (1)...(660) n = A,T,C or G 96 tttttttttt tttttttttt ggaattaaaa gcaatttaat gagggcagag caggaaacat 60 gcatttcttt tcattcgaat cttcagatga accctgagca gccgaagacc agaaaagcca 120 tgaagacttt ctgcttaatt caggggctta caggattctt cagagtgtgt gtgaacaaaa 180 gctttatagt acgtattttt aggatacaaa taagagagag actatggctt ggggtgagaa 240 tgtactgatt acaaggtcta cagacaatta agacacagaa acagatggga agagggtgnc 300 cagcatctgg nggttggctt ctcaagggct tgtctgtgca ccaaattact tctgcttggn 360 cttctgctga gctgggcctg gagtgaccgt tgaaggacat ggctctggta cctttgtgta 420 gcctgncaca ggaactttgg tgtatccttg ctcaggaact ttgatggcac ctggctcagg 480 aaacttgatg aagccttggt caagggacct tgatgcttgc tggctcaggg accttggngn 540 ancctgggct canggacctt tgncncaacc ttggcttcaa gggacccttg gnacatcctg 600 gcnnagggac ccttgggncc aaccctgggc ttnagggacc ctttggntnc nanccttggc 660 97 441 DNA Homo sapien misc_feature (1)...(441) n = A,T,C or G 97 gggaccatac anagtattcc tctcttcaca ccaggaccag ccactgttgc agcatgagtt 60 cccagcagca gaagcagccc tgcatcccac cccctcagct tcagcagcag caggtgaaac 120 agccttgcca gcctccacct caggaaccat gcatccccaa aaccaaggag ccctgccacc 180 ccaaggtgcc tgagccctgc caccccaaag tgcctgagcc ctgccagccc aaggttccag 240 agccatgcca ccccaaggtg cctgagccct gcccttcaat agtcactcca gcaccagccc 300 agcagaanac caagcagaag taatgtggtc cacagccatg cccttgagga gccggccacc 360 agatgctgaa tcccctatcc cattctgtgt atgagtccca tttgccttgc aattagcatt 420 ctgtctcccc caaaaaaaaa a 441 98 600 DNA Homo sapien misc_feature (1)...(600) n = A,T,C or G 98 gtattcctct cttcacacca ggaccagcca ctgttgcagc atgagttccc agcagcagaa 60 gcagccctgc atcccacccc ctcagcttca gcagcagcag gtgaaacagc cttgccagcc 120 tccacctcag gaaccatgca tccccaaaac caaggagccc tgccacccca aggtgcctga 180 gccctgccac cccaaagtgc ctgagccctg ccagcccaag gttccagagc catgccaccc 240 caaggtgcct gagccctgcc cttcaatagt cactccagca ccagcccagc agaanaccaa 300 gcagaagtaa tgtggtccac agccatgccc ttgaggagcc ggccaccana tgctgaatcc 360 cctatcccat tctgtgtatg agtcccattt gccttgcaat tagcattctg tctcccccaa 420 aaaagaatgt gctatgaagc tttctttcct acacactctg agtctctgaa tgaagctgaa 480 ggtcttaant acaganctag ttttcagctg ctcagaattc tctgaagaaa agatttaaga 540 tgaaaggcaa atgattcagc tccttattac cccattaaat tcnctttcaa ttccaaaaaa 600 99 667 DNA Homo sapien misc_feature (1)...(667) n = A,T,C or G 99 actagtgact gagttcctgg caaagaaatt tgacctggac cagttgataa ctcatgtttt 60 accatttaaa aaaatcagtg aaggatttga gctgctcaat tcaggacaaa gcattcgaac 120 ggtcctgacg ttttgagatc caaagtggca ggaggtctgt gttgtcatgg tgaactggag 180 tttctcttgt gagagttccc tcatctgaaa tcatgtatct gtctcacaaa tacaagcata 240 agtagaagat ttgttgaaga catagaaccc ttataaagaa ttattaacct ttataaacat 300 ttaaagtctt gtgagcacct gggaattagt ataataacaa tgttnatatt tttgatttac 360 attttgtaag gctataattg tatcttttaa gaaaacatac cttggatttc tatgttgaaa 420 tggagatttt taagagtttt aaccagctgc tgcagatata ttactcaaaa cagatatagc 480 gtataaagat atagtaaatg catctcctag agtaatattc acttaacaca ttggaaacta 540 ttatttttta gatttgaata tnaatgttat tttttaaaca cttgttatga gttacttggg 600 attacatttt gaaatcagtt cattccatga tgcanattac tgggattaga ttaagaaaga 660 cggaaaa 667 100 583 DNA Homo sapien misc_feature (1)...(583) n = A,T,C or G 100 gttttgtttg taagatgatc acagtcatgt tacactgatc taaaggacat atatataacc 60 ctttaaaaaa aaaatcactg cctcattctt atttcaagat gaatttctat acagactaga 120 tgtttttctg aagatcaatt agacattttg aaaatgattt aaagtgtttt ccttaatgtt 180 ctctgaaaac aagtttcttt tgtagtttta accaaaaaag tgcccttttt gtcactggat 240 tctcctagca ttcatgattt ttttttcata caatgaaatt aaaattgcta aaatcatgga 300 ctggctttct ggttggattt caggtaagat gtgtttaagg ccagagcttt tctcagtatt 360 tgattttttt ccccaatatt tgatttttta aaaatataca catnggtgct gcatttatat 420 ctgctggttt aaaattctgt catatttcac ttctagcctt ttagttatgg caaatcatat 480 tttactttta cttaaagcat ttggtnattt ggantatctg gttctannct aaaaaaanta 540 attctatnaa ttgaantttt ggtactcnnc catatttgga tcc 583 101 592 DNA Homo sapien misc_feature (1)...(592) n = A,T,C or G 101 gtggagacgt acaaagagca gccgctcaag acacctggga agaaaaagaa aggcaagccc 60 gggaaacgca aggagcagga aaagaaaaaa cggcgaactc gctctgcctg gttagactct 120 ggagtgactg ggagtgggct agaaggggac cacctgtctg acacctccac aacgtcgctg 180 gagctcgatt cacggaggca ttgaaatttt cagcaganac cttccaagga catattgcag 240 gattctgtaa tagtgaacat atggaaagta ttagaaatat ttattgtctg taaatactgt 300 aaatgcattg gaataaaact gtctccccca ttgctctatg aaactgcaca ttggtcattg 360 tgaatatttt tttttttgcc aaggctaatc caattattat tatcacattt accataattt 420 attttgtcca ttgatgtatt tattttgtaa atgtatcttg gtgctgctga atttctatat 480 tttttgtaca taatgcnttt anatatacct atcaagtttg ttgataaatg acncaatgaa 540 gtgncncnan ttggnggttg aatttaatga atgcctaatt ttattatccc aa 592 102 587 DNA Homo sapien misc_feature (1)...(587) n = A,T,C or G 102 cgtcctaagc acttagacta catcagggaa gaacacagac cacatccctg tcctcatgcg 60 gcttatgttt tctggaagaa agtggagacc nagtccttgg ctttagggct ccccggctgg 120 gggctgtgca ntccggtcag ggcgggaagg gaaatgcacc gctgcatgtg aacttacagc 180 ccaggcggat gccccttccc ttagcactac ctggcctcct gcatcccctc gcctcatgtt 240 cctcccacct tcaaanaatg aanaacccca tgggcccagc cccttgccct ggggaaccaa 300 ggcagccttc caaaactcag gggctgaagc anactattag ggcaggggct gactttgggt 360 gacactgccc attccctctc agggcagctc angtcacccn ggnctcttga acccagcctg 420 ttcctttgaa aaagggcaaa actgaaaagg gcttttccta naaaaagaaa aaccagggaa 480 ctttgccagg gcttcnntnt taccaaaacn ncttctcnng gatttttaat tccccattng 540 gcctccactt accnggggcn atgccccaaa attaanaatt tcccatc 587 103 496 DNA Homo sapien misc_feature (1)...(496) n = A,T,C or G 103 anaggactgg ccctacntgc tctctctcgt cctacctatc aatgcccaac atggcagaac 60 ctgcanccct tggncactgc anatggaaac ctctcagtgt cttgacatca ccctacccnt 120 gcggtgggtc tccaccacaa ccactttgac tctgtggtcc ctgnanggtg gnttctcctg 180 actggcagga tggaccttan ccnacatatc cctctgttcc ctctgctnag anaaagaatt 240 cccttaacat gatataatcc acccatgcaa ntngctactg gcccagctac catttaccat 300 ttgcctacag aatttcattc agtctacact ttggcattct ctctggcgat agagtgtggc 360 tgggctgacc gcaaaaggtg ccttacacac tggcccccac cctcaaccgt tgacncatca 420 gangcttgcc tcctccttct gattnncccc catgttggat atcagggtgc tcnagggatt 480 ggaaaagaaa caaaac 496 104 575 DNA Homo sapien misc_feature (1)...(575) n = A,T,C or G 104 gcacctgctc tcaatccnnc tctcaccatg atcctccgcc tgcanaaact cctctgccaa 60 ctatggangt ggtttcnggg gtggctcttg ccaactggga agaagccgtg gtgtctctac 120 ctgttcaact cngtttgtgt ctgggggatc aactnggggc tatggaagcg gctnaactgt 180 tgttttggtg gaagggctgg taattggctt tgggaagtng cttatngaag ttggcctngg 240 gaagttgcta ttgaaagtng ccntggaagt ngntttggtg gggggttttg ctggtggcct 300 ttgttnaatt tgggtgcttt gtnaatggcg gccccctcnc ctgggcaatg aaaaaaatca 360 ccnatgcngn aaacctcnac nnaacagcct gggcttccct cacctcgaaa aaagttgctc 420 cccccccaaa aaaggncaan cccctcaann tggaangttg aaaaaatcct cgaatgggga 480 ncccnaaaac aaaaancccc ccntttcccn gnaanggggg aaataccncc cccccactta 540 cnaaaaccct tntaaaaaac cccccgggaa aaaaa 575 105 619 DNA Homo sapien misc_feature (1)...(619) n = A,T,C or G 105 cactagtagg atagaaacac tgtgtcccga gagtaaggag agaagctact attgattaga 60 gcctaaccca ggttaactgc aagaagaggc gggatacttt cagctttcca tgtaactgta 120 tgcataaagc caatgtagtc cagtttctaa gatcatgttc caagctaact gaatcccact 180 tcaatacaca ctcatgaact cctgatggaa caataacagg cccaagcctg tggtatgatg 240 tgcacacttg ctagactcan aaaaaatact actctcataa atgggtggga gtattttggt 300 gacaacctac tttgcttggc tgagtgaagg aatgatattc atatattcat ttattccatg 360 gacatttagt tagtgctttt tatataccag gcatgatgct gagtgacact cttgtgtata 420 tttccaaatt tttgtacagt cgctgcacat atttgaaatc atatattaag acttccaaaa 480 aatgaagtcc ctggtttttc atggcaactt gatcagtaaa ggattcncct ctgtttggta 540 cttaaaacat ctactatatn gttnanatga aattcctttt ccccncctcc cgaaaaaana 600 aagtggtggg gaaaaaaaa 619 106 506 DNA Homo sapien misc_feature (1)...(506) n = A,T,C or G 106 cattggtnct ttcatttgct ntggaagtgt nnatctctaa cagtggacaa agttcccngt 60 gccttaaact ctgtnacact tttgggaant gaaaanttng tantatgata ggttattctg 120 angtanagat gttctggata ccattanatn tgcccccngt gtcagaggct catattgtgt 180 tatgtaaatg gtatntcatt cgctactatn antcaattng aaatanggtc tttgggttat 240 gaatantnng cagcncanct nanangctgt ctgtngtatt cattgtggtc atagcacctc 300 acancattgt aacctcnatc nagtgagaca nactagnaan ttcctagtga tggctcanga 360 ttccaaatgg nctcatntcn aatgtttaaa agttanttaa gtgtaagaaa tacagactgg 420 atgttccacc aactagtacc tgtaatgacn ggcctgtccc aacacatctc ccttttccat 480 gactgtggta ncccgcatcg gaaaaa 506 107 452 DNA Homo sapien misc_feature (1)...(452) n = A,T,C or G 107 gttgagtctg tactaaacag taagatatct caatgaacca taaattcaac tttgtaaaaa 60 tcttttgaag catagataat attgtttggt aaatgtttct tttgtttggt aaatgtttct 120 tttaaagacc ctcctattct ataaaactct gcatgtagag gcttgtttac ctttctctct 180 ctaaggttta caataggagt ggtgatttga aaaatataaa attatgagat tggttttcct 240 gtggcataaa ttgcatcact gtatcatttt cttttttaac cggtaagant ttcagtttgt 300 tggaaagtaa ctgtganaac ccagtttccc gtccatctcc cttagggact acccatagaa 360 catgaaaagg tccccacnga agcaagaaga taagtctttc atggctgctg gttgcttaaa 420 ccactttaaa accaaaaaat tccccttgga aa 452 108 502 DNA Homo sapien misc_feature (1)...(502) n = A,T,C or G 108 atcttcttcc cttaattagt tnttatttat ntattaaatt ttattgcatg tcctggcaaa 60 caaaaagaga ttgtagattg gcttctggct ccccaaaagc ccataacaga aagtaccaca 120 agaccncaac tgaagcttaa aaaatctatc acatgtataa tacctttnga agaacattaa 180 tanagcatat aaaactttta acatntgctt aatgttgtnc aattataaaa ntaatngaaa 240 aaaatgtccc tttaacatnc aatatcccac atagtgttat ttnaggggat taccnngnaa 300 naaaaaaagg gtagaaggga tttaatgaaa actctgcttn ccatttctgt ttanaaacgt 360 ctccagaaca aaaacttntc aantctttca gctaaccgca tttgagctna ggccactcaa 420 aaactccatt agncccactt tctaanggtc tctanagctt actaancctt ttgacccctt 480 accctggnta ctcctgccct ca 502 109 1308 DNA Homo sapien 109 acccgaggtc tcgctaaaat catcatggat tcacttggcg ccgtcagcac tcgacttggg 60 tttgatcttt tcaaagagct gaagaaaaca aatgatggca acatcttctt ttcccctgtg 120 ggcatcttga ctgcaattgg catggtcctc ctggggaccc gaggagccac cgcttcccag 180 ttggaggagg tgtttcactc tgaaaaagag acgaagagct caagaataaa ggctgaagaa 240 aaagaggtga ttgagaacac agaagcagta catcaacaat tccaaaagtt tttgactgaa 300 ataagcaaac tcactaatga ttatgaactg aacataacca acaggctgtt tggagaaaaa 360 acatacctct tccttcaaaa atacttagat tatgttgaaa aatattatca tgcatctctg 420 gaacctgttg attttgtaaa tgcagccgat gaaagtcgaa agaagattaa ttcctgggtt 480 gaaagcaaaa caaatgaaaa aatcaaggac ttgttcccag atggctctat tagtagctct 540 accaagctgg tgctggtgaa catggtttat tttaaagggc aatgggacag ggagtttaag 600 aaagaaaata ctaaggaaga gaaattttgg atgaataaga gcacaagtaa atctgtacag 660 atgatgacac agagccattc ctttagcttc actttcctgg aggacttgca ggccaaaatt 720 ctagggattc catataaaaa caacgaccta agcatgtttg tgcttctgcc caacgacatc 780 gatggcctgg agaagataat agataaaata agtcctgaga aattggtaga gtggactagt 840 ccagggcata tggaagaaag aaaggtgaat ctgcacttgc cccggtttga ggtggaggac 900 agttacgatc tagaggcggt cctggctgcc atggggatgg gcgatgcctt cagtgagcac 960 aaagccgact actcgggaat gtcgtcaggc tccgggttgt acgcccagaa gttcctgcac 1020 agttcctttg tggcagtaac tgaggaaggc accgaggctg cagctgccac tggcataggc 1080 tttactgtca catccgcccc aggtcatgaa aatgttcact gcaatcatcc cttcctgttc 1140 ttcatcaggc acaatgaatc caacagcatc ctcttcttcg gcagattttc ttctccttaa 1200 gatgatcgtt gccatggcat tgctgctttt agcaaaaaac aactaccagt gttactcata 1260 tgattatgaa aatcgtccat tcttttaaat ggtggctcac ttgcattt 1308 110 391 PRT Homo sapien 110 Met Asp Ser Leu Gly Ala Val Ser Thr Arg Leu Gly Phe Asp Leu Phe 1 5 10 15 Lys Glu Leu Lys Lys Thr Asn Asp Gly Asn Ile Phe Phe Ser Pro Val 20 25 30 Gly Ile Leu Thr Ala Ile Gly Met Val Leu Leu Gly Thr Arg Gly Ala 35 40 45 Thr Ala Ser Gln Leu Glu Glu Val Phe His Ser Glu Lys Glu Thr Lys 50 55 60 Ser Ser Arg Ile Lys Ala Glu Glu Lys Glu Val Ile Glu Asn Thr Glu 65 70 75 80 Ala Val His Gln Gln Phe Gln Lys Phe Leu Thr Glu Ile Ser Lys Leu 85 90 95 Thr Asn Asp Tyr Glu Leu Asn Ile Thr Asn Arg Leu Phe Gly Glu Lys 100 105 110 Thr Tyr Leu Phe Leu Gln Lys Tyr Leu Asp Tyr Val Glu Lys Tyr Tyr 115 120 125 His Ala Ser Leu Glu Pro Val Asp Phe Val Asn Ala Ala Asp Glu Ser 130 135 140 Arg Lys Lys Ile Asn Ser Trp Val Glu Ser Lys Thr Asn Glu Lys Ile 145 150 155 160 Lys Asp Leu Phe Pro Asp Gly Ser Ile Ser Ser Ser Thr Lys Leu Val 165 170 175 Leu Val Asn Met Val Tyr Phe Lys Gly Gln Trp Asp Arg Glu Phe Lys 180 185 190 Lys Glu Asn Thr Lys Glu Glu Lys Phe Trp Met Asn Lys Ser Thr Ser 195 200 205 Lys Ser Val Gln Met Met Thr Gln Ser His Ser Phe Ser Phe Thr Phe 210 215 220 Leu Glu Asp Leu Gln Ala Lys Ile Leu Gly Ile Pro Tyr Lys Asn Asn 225 230 235 240 Asp Leu Ser Met Phe Val Leu Leu Pro Asn Asp Ile Asp Gly Leu Glu 245 250 255 Lys Ile Ile Asp Lys Ile Ser Pro Glu Lys Leu Val Glu Trp Thr Ser 260 265 270 Pro Gly His Met Glu Glu Arg Lys Val Asn Leu His Leu Pro Arg Phe 275 280 285 Glu Val Glu Asp Ser Tyr Asp Leu Glu Ala Val Leu Ala Ala Met Gly 290 295 300 Met Gly Asp Ala Phe Ser Glu His Lys Ala Asp Tyr Ser Gly Met Ser 305 310 315 320 Ser Gly Ser Gly Leu Tyr Ala Gln Lys Phe Leu His Ser Ser Phe Val 325 330 335 Ala Val Thr Glu Glu Gly Thr Glu Ala Ala Ala Ala Thr Gly Ile Gly 340 345 350 Phe Thr Val Thr Ser Ala Pro Gly His Glu Asn Val His Cys Asn His 355 360 365 Pro Phe Leu Phe Phe Ile Arg His Asn Glu Ser Asn Ser Ile Leu Phe 370 375 380 Phe Gly Arg Phe Ser Ser Pro 385 390 111 1419 DNA Homo sapien 111 ggagaactat aaattaagga tcccagctac ttaattgact tatgcttcct agttcgttgc 60 ccagccacca ccgtctctcc aaaaacccga ggtctcgcta aaatcatcat ggattcactt 120 ggcgccgtca gcactcgact tgggtttgat cttttcaaag agctgaagaa aacaaatgat 180 ggcaacatct tcttttcccc tgtgggcatc ttgactgcaa ttggcatggt cctcctgggg 240 acccgaggag ccaccgcttc ccagttggag gaggtgtttc actctgaaaa agagacgaag 300 agctcaagaa taaaggctga agaaaaagag gtggtaagaa taaaggctga aggaaaagag 360 attgagaaca cagaagcagt acatcaacaa ttccaaaagt ttttgactga aataagcaaa 420 ctcactaatg attatgaact gaacataacc aacaggctgt ttggagaaaa aacatacctc 480 ttccttcaaa aatacttaga ttatgttgaa aaatattatc atgcatctct ggaacctgtt 540 gattttgtaa atgcagccga tgaaagtcga aagaagatta attcctgggt tgaaagcaaa 600 acaaatgaaa aaatcaagga cttgttccca gatggctcta ttagtagctc taccaagctg 660 gtgctggtga acatggttta ttttaaaggg caatgggaca gggagtttaa gaaagaaaat 720 actaaggaag agaaattttg gatgaataag agcacaagta aatctgtaca gatgatgaca 780 cagagccatt cctttagctt cactttcctg gaggacttgc aggccaaaat tctagggatt 840 ccatataaaa acaacgacct aagcatgttt gtgcttctgc ccaacgacat cgatggcctg 900 gagaagataa tagataaaat aagtcctgag aaattggtag agtggactag tccagggcat 960 atggaagaaa gaaaggtgaa tctgcacttg ccccggtttg aggtggagga cagttacgat 1020 ctagaggcgg tcctggctgc catggggatg ggcgatgcct tcagtgagca caaagccgac 1080 tactcgggaa tgtcgtcagg ctccgggttg tacgcccaga agttcctgca cagttccttt 1140 gtggcagtaa ctgaggaagg caccgaggct gcagctgcca ctggcatagg ctttactgtc 1200 acatccgccc caggtcatga aaatgttcac tgcaatcatc ccttcctgtt cttcatcagg 1260 cacaatgaat ccaacagcat cctcttcttc ggcagatttt cttctcctta agatgatcgt 1320 tgccatggca ttgctgcttt tagcaaaaaa caactaccag tgttactcat atgattatga 1380 aaatcgtcca ttcttttaaa tggtggctca cttgcattt 1419 112 400 PRT Homo sapien 112 Met Asp Ser Leu Gly Ala Val Ser Thr Arg Leu Gly Phe Asp Leu Phe 1 5 10 15 Lys Glu Leu Lys Lys Thr Asn Asp Gly Asn Ile Phe Phe Ser Pro Val 20 25 30 Gly Ile Leu Thr Ala Ile Gly Met Val Leu Leu Gly Thr Arg Gly Ala 35 40 45 Thr Ala Ser Gln Leu Glu Glu Val Phe His Ser Glu Lys Glu Thr Lys 50 55 60 Ser Ser Arg Ile Lys Ala Glu Glu Lys Glu Val Val Arg Ile Lys Ala 65 70 75 80 Glu Gly Lys Glu Ile Glu Asn Thr Glu Ala Val His Gln Gln Phe Gln 85 90 95 Lys Phe Leu Thr Glu Ile Ser Lys Leu Thr Asn Asp Tyr Glu Leu Asn 100 105 110 Ile Thr Asn Arg Leu Phe Gly Glu Lys Thr Tyr Leu Phe Leu Gln Lys 115 120 125 Tyr Leu Asp Tyr Val Glu Lys Tyr Tyr His Ala Ser Leu Glu Pro Val 130 135 140 Asp Phe Val Asn Ala Ala Asp Glu Ser Arg Lys Lys Ile Asn Ser Trp 145 150 155 160 Val Glu Ser Lys Thr Asn Glu Lys Ile Lys Asp Leu Phe Pro Asp Gly 165 170 175 Ser Ile Ser Ser Ser Thr Lys Leu Val Leu Val Asn Met Val Tyr Phe 180 185 190 Lys Gly Gln Trp Asp Arg Glu Phe Lys Lys Glu Asn Thr Lys Glu Glu 195 200 205 Lys Phe Trp Met Asn Lys Ser Thr Ser Lys Ser Val Gln Met Met Thr 210 215 220 Gln Ser His Ser Phe Ser Phe Thr Phe Leu Glu Asp Leu Gln Ala Lys 225 230 235 240 Ile Leu Gly Ile Pro Tyr Lys Asn Asn Asp Leu Ser Met Phe Val Leu 245 250 255 Leu Pro Asn Asp Ile Asp Gly Leu Glu Lys Ile Ile Asp Lys Ile Ser 260 265 270 Pro Glu Lys Leu Val Glu Trp Thr Ser Pro Gly His Met Glu Glu Arg 275 280 285 Lys Val Asn Leu His Leu Pro Arg Phe Glu Val Glu Asp Ser Tyr Asp 290 295 300 Leu Glu Ala Val Leu Ala Ala Met Gly Met Gly Asp Ala Phe Ser Glu 305 310 315 320 His Lys Ala Asp Tyr Ser Gly Met Ser Ser Gly Ser Gly Leu Tyr Ala 325 330 335 Gln Lys Phe Leu His Ser Ser Phe Val Ala Val Thr Glu Glu Gly Thr 340 345 350 Glu Ala Ala Ala Ala Thr Gly Ile Gly Phe Thr Val Thr Ser Ala Pro 355 360 365 Gly His Glu Asn Val His Cys Asn His Pro Phe Leu Phe Phe Ile Arg 370 375 380 His Asn Glu Ser Asn Ser Ile Leu Phe Phe Gly Arg Phe Ser Ser Pro 385 390 395 400 113 957 DNA Homo sapien 113 ctcgaccttc tctgcacagc ggatgaaccc tgagcagctg aagaccagaa aagccactat 60 gactttctgc ttaattcagg agcttacagg attcttcaaa gagtgtgtcc agcatccttt 120 gaaacatgag ttcttaccag cagaagcaga cctttacccc accacctcag cttcaacagc 180 agcaggtgaa acaacccagc cagcctccac ctcaggaaat atttgttccc acaaccaagg 240 agccatgcca ctcaaaggtt ccacaacctg gaaacacaaa gattccagag ccaggctgta 300 ccaaggtccc tgagccaggc tgtaccaagg tccctgagcc aggttgtacc aaggtccctg 360 agccaggatg taccaaggtc cctgagccag gttgtaccaa ggtccctgag ccaggctaca 420 ccaaggtccc tgagccaggc agcatcaagg tccctgacca aggcttcatc aagtttcctg 480 agccaggtgc catcaaagtt cctgagcaag gatacaccaa agttcctgtg ccaggctaca 540 caaaggtacc agagccatgt ccttcaacgg tcactccagg cccagctcag cagaagacca 600 agcagaagta atttggtgca cagacaagcc cttgagaagc caaccaccag atgctggaca 660 ccctcttccc atctgtttct gtgtcttaat tgtctgtaga ccttgtaatc agtacattct 720 caccccaagc catagtctct ctcttatttg tatcctaaaa atacggtact ataaagcttt 780 tgttcacaca cactctgaag aatcctgtaa gcccctgaat taagcagaaa gtcttcatgg 840 cttttctggt cttcggctgc tcagggttca tctgaagatt cgaatgaaaa gaaatgcatg 900 tttcctgctc tgccctcatt aaattgcttt taattccaaa aaaaaaaaaa aaaaaaa 957 114 161 PRT Homo sapien 114 Met Ser Ser Tyr Gln Gln Lys Gln Thr Phe Thr Pro Pro Pro Gln Leu 1 5 10 15 Gln Gln Gln Gln Val Lys Gln Pro Ser Gln Pro Pro Pro Gln Glu Ile 20 25 30 Phe Val Pro Thr Thr Lys Glu Pro Cys His Ser Lys Val Pro Gln Pro 35 40 45 Gly Asn Thr Lys Ile Pro Glu Pro Gly Cys Thr Lys Val Pro Glu Pro 50 55 60 Gly Cys Thr Lys Val Pro Glu Pro Gly Cys Thr Lys Val Pro Glu Pro 65 70 75 80 Gly Cys Thr Lys Val Pro Glu Pro Gly Cys Thr Lys Val Pro Glu Pro 85 90 95 Gly Tyr Thr Lys Val Pro Glu Pro Gly Ser Ile Lys Val Pro Asp Gln 100 105 110 Gly Phe Ile Lys Phe Pro Glu Pro Gly Ala Ile Lys Val Pro Glu Gln 115 120 125 Gly Tyr Thr Lys Val Pro Val Pro Gly Tyr Thr Lys Val Pro Glu Pro 130 135 140 Cys Pro Ser Thr Val Thr Pro Gly Pro Ala Gln Gln Lys Thr Lys Gln 145 150 155 160 Lys 115 506 DNA Homo sapien misc_feature (1)...(506) n = A,T,C or G 115 cattggtnct ttcatttgct ntggaagtgt nnatctctaa cagtggacaa agttcccngt 60 gccttaaact ctgtnacact tttgggaant gaaaanttng tantatgata ggttattctg 120 angtanagat gttctggata ccattanatn tgcccccngt gtcagaggct catattgtgt 180 tatgtaaatg gtatntcatt cgctactatn antcaattng aaatanggtc tttgggttat 240 gaatantnng cagcncanct nanangctgt ctgtngtatt cattgtggtc atagcacctc 300 acancattgt aacctcnatc nagtgagaca nactagnaan ttcctagtga tggctcanga 360 ttccaaatgg nctcatntcn aatgtttaaa agttanttaa gtgtaagaaa tacagactgg 420 atgttccacc aactagtacc tgtaatgacn ggcctgtccc aacacatctc ccttttccat 480 gactgtggta ncccgcatcg gaaaaa 506 116 3079 DNA Homo sapien 116 ggatccccgg gtttcctaaa ccccccacag agtcctgccc aggccaaaga gcaaggaaaa 60 ggtcaaaggg cagaaaaaat gctgagttag gaggagctat ggaaggataa acctggcctt 120 aaagaggtca aagtggttta tagggggcgc tgagggcttc ccacattctc tggcctaaac 180 cttgcaggca gatctgccca gtgggctctg ggatagctgt gccttcccta acaaaaaaat 240 tgtgcacaaa aggatgaaac tctattttcc ctctagcaca taaccaagaa tataaggcta 300 cagattgcct ttcccagagg gaaaaccctg cagcaacctg ctgcctggaa aagtgtaaga 360 gcagatcact ggggaatcgt ttgccccccg ctgatggaca gcttccccaa gctccaaggg 420 caggtgctca gcatgtaccg tactgggatg gttgtcaata ctcctggtcc tgtaagagtc 480 ccaggacact gccatgccaa tgccccctca gttcctggca tcctttttgg gctgctcaca 540 gccccagcct ctatggtgaa gacatacttg ctagcagcgt caccaacttg ttgccaagag 600 atcagtgctc gaaggcaagg ttatttctaa ctgagcagag cctgccagga agaaagcgtt 660 tgcaccccac accactgtgc aggtgtgacc ggtgagctca cagctgcccc ccaggcatgc 720 ccagcccact taatcatcac agctcgacag ctctctcgcc cagcccagtt ctggaaggga 780 taaaaagggg catcaccgtt cctgggtaac agagccacct tctgcgtcct gctgagctct 840 gttctctcca gcacctccca acccactagt gcctggttct cttgctccac caggaacaag 900 ccaccatgtc tcgccagtca agtgtgtctt ccggagcggg gggcagtcgt agcttcagca 960 ccgcctctgc catcaccccg tctgtctccc gcaccagctt cacctccgtg tcccggtccg 1020 ggggtggcgg tggtggtggc ttcggcaggg tcagccttgc gggtgcttgt ggagtgggtg 1080 gctatggcag ccggagcctc tacaacctgg ggggctccaa gaggatatcc atcagcacta 1140 gtggtggcag cttcaggaac cggtttggtg ctggtgctgg aggcggctat ggctttggag 1200 gtggtgccgg tagtggattt ggtttcggcg gtggagctgg tggtggcttt gggctcggtg 1260 gcggagctgg ctttggaggt ggcttcggtg gccctggctt tcctgtctgc cctcctggag 1320 gtatccaaga ggtcactgtc aaccagagtc tcctgactcc cctcaacctg caaatcgacc 1380 ccagcatcca gagggtgagg accgaggagc gcgagcagat caagaccctc aacaataagt 1440 ttgcctcctt catcgacaag gtgcggttcc tggagcagca gaacaaggtt ctggaaacaa 1500 agtggaccct gctgcaggag cagggcacca agactgtgag gcagaacctg gagccgttgt 1560 tcgagcagta catcaacaac ctcaggaggc agctggacag catcgtgggg gaacggggcc 1620 gcctggactc agagctgaga aacatgcagg acctggtgga agacttcaag aacaagtatg 1680 aggatgaaat caacaagcgt accactgctg agaatgagtt tgtgatgctg aagaaggatg 1740 tagatgctgc ctacatgaac aaggtggagc tggaggccaa ggttgatgca ctgatggatg 1800 agattaactt catgaagatg ttctttgatg cggagctgtc ccagatgcag acgcatgtct 1860 ctgacacctc agtggtcctc tccatggaca acaaccgcaa cctggacctg gatagcatca 1920 tcgctgaggt caaggcccag tatgaggaga ttgccaaccg cagccggaca gaagccgagt 1980 cctggtatca gaccaagtat gaggagctgc agcagacagc tggccggcat ggcgatgacc 2040 tccgcaacac caagcatgag atctctgaga tgaaccggat gatccagagg ctgagagccg 2100 agattgacaa tgtcaagaaa cagtgcgcca atctgcagaa cgccattgcg gatgccgagc 2160 agcgtgggga gctggccctc aaggatgcca ggaacaagct ggccgagctg gaggaggccc 2220 tgcagaaggc caagcaggac atggcccggc tgctgcgtga gtaccaggag ctcatgaaca 2280 ccaagctggc cctggacgtg gagatcgcca cttaccgcaa gctgctggag ggcgaggaat 2340 gcagactcag tggagaagga gttggaccag tcaacatctc tgttgtcaca agcagtgttt 2400 cctctggata tggcagtggc agtggctatg gcggtggcct cggtggaggt cttggcggcg 2460 gcctcggtgg aggtcttgcc ggaggtagca gtggaagcta ctactccagc agcagtgggg 2520 gtgtcggcct aggtggtggg ctcagtgtgg ggggctctgg cttcagtgca agcagtagcc 2580 gagggctggg ggtgggcttt ggcagtggcg ggggtagcag ctccagcgtc aaatttgtct 2640 ccaccacctc ctcctcccgg aagagcttca agagctaaga acctgctgca agtcactgcc 2700 ttccaagtgc agcaacccag cccatggaga ttgcctcttc taggcagttg ctcaagccat 2760 gttttatcct tttctggaga gtagtctaga ccaagccaat tgcagaacca cattctttgg 2820 ttcccaggag agccccattc ccagcccctg gtctcccgtg ccgcagttct atattctgct 2880 tcaaatcagc cttcaggttt cccacagcat ggcccctgct gacacgagaa cccaaagttt 2940 tcccaaatct aaatcatcaa aacagaatcc ccaccccaat cccaaatttt gttttggttc 3000 taactacctc cagaatgtgt tcaataaaat gttttataat ataagctggt gtgcagaatt 3060 gttttttttt tctacccaa 3079 117 6921 DNA Homo sapien 117 aattctgac tgtccactca aaacttctat tccgatcaaa gctatctgtg actacagaca 60 attgagata accatttaca aagacgatga atgtgttttg gcgaataact ctcatcgtgc 120 aaatggaag gtcattagtc ctactgggaa tgaggctatg gtcccatctg tgtgcttcac 180 gttcctcca ccaaacaaag aagcggtgga ccttgccaac agaattgagc aacagtatca 240 aatgtcctg actctttggc atgagtctca cataaacatg aagagtgtag tatcctggca 300 tatctcatc aatgaaattg atagaattcg agctagcaat gtggcttcaa taaagacaat 360 ctacctggt gaacatcagc aagttctaag taatctacaa tctcgttttg aagattttct 420 gaagatagc caggaatccc aagtcttttc aggctcagat ataacacaac tggaaaagga 480 gttaatgta tgtaagcagt attatcaaga acttcttaaa tctgcagaaa gagaggagca 540 gaggaatca gtttataatc tctacatctc tgaagttcga aacattagac ttcggttaga 600 aactgtgaa gatcggctga ttagacagat tcgaactccc ctggaaagag atgatttgca 660 gaaagtgtg ttcagaatca cagaacagga gaaactaaag aaagagctgg aacgacttaa 720 gatgatttg ggaacaatca caaataagtg tgaggagttt ttcagtcaag cagcagcctc 780 tcatcagtc cctaccctac gatcagagct taatgtggtc cttcagaaca tgaaccaagt 840 tattctatg tcttccactt acatagataa gttgaaaact gttaacttgg tgttaaaaaa 900 actcaagct gcagaagccc tcgtaaaact ctatgaaact aaactgtgtg aagaagaagc 960 gttatagct gacaagaata atattgagaa tctaataagt actttaaagc aatggagatc 1020 gaagtagat gaaaagagac aggtattcca tgccttagag gatgagttgc agaaagctaa 1080 gccatcagt gatgaaatgt ttaaaacgta taaagaacgg gaccttgatt ttgactggca 1140 aaagaaaaa gcagatcaat tagttgaaag gtggcaaaat gttcatgtgc agattgacaa 1200 aggttacgg gacttagagg gcattggcaa atcactgaag tactacagag acacttacca 1260 cctttagat gattggatcc agcaggttga aactactcag agaaagattc aggaaaatca 1320 cctgaaaat agtaaaaccc tagccacaca gttgaatcaa cagaagatgc tggtgtccga 1380 atagaaatg aaacagagca aaatggacga gtgtcaaaaa tatgcagaac agtactcagc 1440 acagtgaag gactatgaat tacaaacaat gacctaccgg gccatggtag attcacaaca 1500 aaatctcca gtgaaacgcc gaagaatgca gagttcagca gatctcatta ttcaagagtt 1560 atggaccta aggactcgat atactgccct ggtcactctc atgacacaat atattaaatt 1620 gctggtgat tcattgaaga ggctggaaga ggaggagatt aaaaggtgta aggagacttc 1680 gaacatggg gcatattcag atctgcttca gcgtcagaag gcaacagtgc ttgagaatag 1740 aaacttaca ggaaagataa gtgagttgga aagaatggta gctgaactaa agaaacaaaa 1800 tcccgagta gaggaagaac ttccgaaggt cagggaggct gcagaaaatg aattgagaaa 1860 cagcagaga aatgtagaag atatctctct gcagaagata agggctgaaa gtgaagccaa 1920 cagtaccgc agggaacttg aaaccattgt gagagagaag gaagccgctg aaagagaact 1980 gagcgggtg aggcagctca ccatagaggc cgaggctaaa agagctgccg tggaagagaa 2040 ctcctgaat tttcgcaatc agttggagga aaacaccttt accagacgaa cactggaaga 2100 catcttaaa agaaaagatt taagtctcaa tgatttggag caacaaaaaa ataaattaat 2160 gaagaatta agaagaaaga gagacaatga ggaagaactc ttgaagctga taaagcagat 2220 gaaaaagac cttgcatttc agaaacaggt agcagagaaa cagttgaaag aaaagcagaa 2280 attgaattg gaagcaagaa gaaaaataac tgaaattcag tatacatgta gagaaaatgc 2340 ttgccagtg tgtccgatca cacaggctac atcatgcagg gcagtaacgg gtctccagca 2400 gaacatgac aagcagaaag cagaagaact caaacagcag gtagatgaac taacagctgc 2460 aatagaaag gctgaacaag acatgagaga gctgacatat gaacttaatg ccctccagct 2520 gaaaaaacg tcatctgagg aaaaggctcg tttgctaaaa gataaactag atgaaacaaa 2580 aatacactc agatgcctta agttggagct ggaaaggaag gatcaggcgg agaaagggta 2640 tctcaacaa ctcagagagc ttggtaggca attgaatcaa accacaggta aagctgaaga 2700 gccatgcaa gaagctagtg atctcaagaa aataaagcgc aattatcagt tagaattaga 2760 tctcttaat catgaaaaag ggaaactaca aagagaagta gacagaatca caagggcaca 2820 gctgtagct gagaagaata ttcagcattt aaattcacaa attcattctt ttcgagatga 2880 aaagaatta gaaagactac aaatctgcca gagaaaatca gatcatctaa aagaacaatt 2940 gagaaaagc catgagcagt tgcttcaaaa tatcaaagct gaaaaagaaa ataatgataa 3000 atccaaagg ctcaatgaag aattggagaa aagtaatgag tgtgcagaga tgctaaaaca 3060 aaagtagag gagcttacta ggcagaataa tgaaaccaaa ttaatgatgc agagaattca 3120 gcagaatca gagaatatag ttttagagaa acaaactatc cagcaaagat gtgaagcact 3180 aaaattcag gcagatggtt ttaaagatca gctacgcagc acaaatgaac acttgcataa 3240 cagacaaaa acagagcagg attttcaaag aaaaattaaa tgcctagaag aagacctggc 3300 aaaagtcaa aatttggtaa gtgaatttaa gcaaaagtgt gaccaacaga acattatcat 3360 cagaatacc aagaaagaag ttagaaatct gaatgcggaa ctgaatgctt ccaaagaaga 3420 aagcgacgc ggggagcaga aagttcagct acaacaagct caggtgcaag agttaaataa 3480 aggttgaaa aaagtacaag acgaattaca cttaaagacc atagaggagc agatgaccca 3540 agaaagatg gttctgtttc aggaagaatc tggtaaattc aaacaatcag cagaggagtt 3600 cggaagaag atggaaaaat taatggagtc caaagtcatc actgaaaatg atatttcagg 3660 attaggctt gactttgtgt ctcttcaaca agaaaactct agagcccaag aaaatgctaa 3720 ctttgtgaa acaaacatta aagaacttga aagacagctt caacagtatc gtgaacaaat 3780 cagcaaggg cagcacatgg aagcaaatca ttaccaaaaa tgtcagaaac ttgaggatga 3840 ctgatagcc cagaagcgtg aggttgaaaa cctgaagcaa aaaatggacc aacagatcaa 3900 gagcatgaa catcaattag ttttgctcca gtgtgaaatt caaaaaaaga gcacagccaa 3960 gactgtacc ttcaaaccag attttgagat gacagtgaag gagtgccagc actctggaga 4020 ctgtcctct agaaacactg gacaccttca cccaacaccc agatcccctc tgttgagatg 4080 actcaagaa ccacagccat tggaagagaa gtggcagcat cgggttgttg aacagatacc 4140 aaagaagtc caattccagc caccaggggc tccactcgag aaagagaaaa gccagcagtg 4200 tactctgag tacttttctc agacaagcac cgagttacag ataacttttg atgagacaaa 4260 cccattaca agactgtctg aaattgagaa gataagagac caagccctga acaattctag 4320 ccacctgtt aggtatcaag ataacgcatg tgaaatggaa ctggtgaagg ttttgacacc 4380 ttagagata gctaagaaca agcagtatga tatgcataca gaagtcacaa cattaaaaca 4440 gaaaagaac ccagttccca gtgctgaaga atggatgctt gaagggtgca gagcatctgg 4500 ggactcaag aaaggggatt tccttaagaa gggcttagaa ccagagacct tccagaactt 4560 gatggtgat catgcatgtt cagtcaggga tgatgaattt aaattccaag ggcttaggca 4620 actgtgact gccaggcagt tggtggaagc taagcttctg gacatgagaa caattgagca 4680 ctgcgactc ggtcttaaga ctgttgaaga agttcagaaa actcttaaca agtttctgac 4740 aaagccacc tcaattgcag ggctttacct agaatctaca aaagaaaaga tttcatttgc 4800 tcagcggcc gagagaatca taatagacaa aatggtggct ttggcatttt tagaagctca 4860 gctgcaaca ggttttataa ttgatcccat ttcaggtcag acatattctg ttgaagatgc 4920 gttcttaaa ggagttgttg accccgaatt cagaattagg cttcttgagg cagagaaggc 4980 gctgtggga tattcttatt cttctaagac attgtcagtg tttcaagcta tggaaaatag 5040 atgcttgac agacaaaaag gtaaacatat cttggaagcc cagattgcca gtgggggtgt 5100 attgaccct gtgagaggca ttcgtgttcc tccagaaatt gctctgcagc aggggttgtt 5160 aataatgcc atcttacagt ttttacatga gccatccagc aacacaagag ttttccctaa 5220 cccaataac aagcaagctc tgtattactc agaattactg cgaatgtgtg tatttgatgt 5280 gagtcccaa tgctttctgt ttccatttgg ggagaggaac atttccaatc tcaatgtcaa 5340 aaaacacat agaatttctg tagtagatac taaaacagga tcagaattga ccgtgtatga 5400 gctttccag agaaacctga ttgagaaaag tatatatctt gaactttcag ggcagcaata 5460 cagtggaag gaagctatgt tttttgaatc ctatgggcat tcttctcata tgctgactga 5520 actaaaaca ggattacact tcaatattaa tgaggctata gagcagggaa caattgacaa 5580 gccttggtc aaaaagtatc aggaaggcct catcacactt acagaacttg ctgattcttt 5640 ctgagccgg ttagtcccca agaaagattt gcacagtcct gttgcagggt attggctgac 5700 gctagtggg gaaaggatct ctgtactaaa agcctcccgt agaaatttgg ttgatcggat 5760 actgccctc cgatgccttg aagcccaagt cagtacaggg ggcataattg atcctcttac 5820 ggcaaaaag taccgggtgg ccgaagcttt gcatagaggc ctggttgatg aggggtttgc 5880 cagcagctg cgacagtgtg aattagtaat cacagggatt ggccatccca tcactaacaa 5940 atgatgtca gtggtggaag ctgtgaatgc aaatattata aataaggaaa tgggaatccg 6000 tgtttggaa tttcagtact tgacaggagg gttgatagag ccacaggttc actctcggtt 6060 tcaatagaa gaggctctcc aagtaggtat tatagatgtc ctcattgcca caaaactcaa 6120 gatcaaaag tcatatgtca gaaatataat atgccctcag acaaaaagaa agttgacata 6180 aaagaagcc ttagaaaaag ctgattttga tttccacaca ggacttaaac tgttagaagt 6240 tctgagccc ctgatgacag gaatttctag cctctactat tcttcctaat gggacatgtt 6300 aaataactg tgcaaggggt gatgcaggct ggttcatgcc actttttcag agtatgatga 6360 atcggctac atatgcagtc tgtgaattat gtaacatact ctatttcttg agggctgcaa 6420 ttgctaagt gctcaaaata gagtaagttt taaattgaaa attacataag atttaatgcc 6480 ttcaaatgg tttcatttag ccttgagaat ggttttttga aacttggcca cactaaaatg 6540 ttttttttt tttacgtaga atgtgggata aacttgatga actccaagtt cacagtgtca 6600 ttcttcaga actccccttc attgaatagt gatcatttat taaatgataa attgcactcg 6660 tgaaagagc acgtcatgaa gcaccatgga atcaaagaga aagatataaa ttcgttccca 6720 agccttcaa gctgcagtgt tttagattgc ttcaaaaaat gaaaaagttt tgcctttttc 6780 atatagtga ccttctttgc atattaaaat gtttaccaca atgtcccatt tctagttaag 6840 cttcgcact tgaaagctaa cattatgaat attatgtgtt ggaggagggg aaggattttc 6900 tcattctgt gtattttccg g 6921 118 946 DNA Homo sapien 118 cttctgactg ggctcaggct gacaggtaga gctcaccatg gcttcttgtg tccttgtccc 60 ctccccatca cagctgtggt gcagtccacc gtctccagtg gctatggcgg tgccagtggt 120 gtcggcagtg gcttaggcct gggtggagga agcagctact cctatggcag tggtcttggc 180 gttggaggtg gcttcagttc cagcagtggc agagccattg ggggtggcct cagctctgtt 240 ggaggcggca gttccaccat caagtacacc accacctcct cctccagcag gaagagctat 300 aagcactaaa gtgcgtctgc tagctctcgg tcccacagtc ctcaggcccc tctctggctg 360 cagagccctc tcctcaggtt gcctgtcctc tcctggcctc cagtctcccc tgctgtccca 420 ggtagagctg gggatgaatg cttagtgccc tcacttcttc tctctctctc tataccatct 480 gagcacccat tgctcaccat cagatcaacc tctgatttta catcatgatg taatcaccac 540 tggagcttca ctgttactaa attattaatt tcttgcctcc agtgttctat ctctgaggct 600 gagcattata agaaaatgac ctctgctcct tttcattgca gaaaattgcc aggggcttat 660 ttcagaacaa cttccactta ctttccactg gctctcaaac tctctaactt ataagtgttg 720 tgaaccccca cccaggcagt atccatgaaa gcacaagtga ctagtcctat gatgtacaaa 780 gcctgtatct ctgtgatgat ttctgtgctc ttcactgttt gcaattgcta aataaagcag 840 atttataata catatattct tttactttgc cttgctttgg ggccaaagtt ttgggcttaa 900 acttttttat ctgataagtg aatagttgtt tttaaaagat aatcta 946 119 8948 DNA Homo sapien 119 caacagccc ctgctccttg ggcccctcca tgccatgccg taatctctcc cacccgacca 60 caccaacac ccagctccga cgcagctcct ctgcgccctt gccgccctcc gagccacagc 120 ttcctcccg ctcctgcccc cggcccgtcg ccgtctccgc gctcgcagcg gcctcgggag 180 gcccaggta gcgagcagcg acctcgcgag ccttccgcac tcccgcccgg ttccccggcc 240 tccgcctat ccttggcccc ctccgctttc tccgcgccgg cccgcctcgc ttatgcctcg 300 cgctgagcc gctctcccga ttgcccgccg acatgagctg caacggaggc tcccacccgc 360 gatcaacac tctgggccgc atgatccgcg ccgagtctgg cccggacctg cgctacgagg 420 gaccagcgg cggcgggggc accagcagga tgtactattc tcggcgcggc gtgatcaccg 480 ccagaactc ggacggctac tgtcaaaccg gcacgatgtc caggcaccag aaccagaaca 540 catccagga gctgctgcag aactgctccg actgcttgat gcgagcagag ctcatcgtgc 600 gcctgaatt gaagtatgga gatggaatac aactgactcg gagtcgagaa ttggatgagt 660 ttttgccca ggccaatgac caaatggaaa tcctcgacag cttgatcaga gagatgcggc 720 gatgggcca gccctgtgat gcttaccaga aaaggcttct tcagctccaa gagcaaatgc 780 agcccttta taaagccatc agtgtccctc gagtccgcag ggccagctcc aagggtggtg 840 aggctacac ttgtcagagt ggctctggct gggatgagtt caccaaacat gtcaccagtg 900 atgtttggg gtggatgagg cagcaaaggg cggagatgga catggtggcc tggggtgtgg 960 cctggcctc agtggagcag cacattaaca gccaccgggg catccacaac tccatcggcg 1020 ctatcgctg gcagctggac aaaatcaaag ccgacctgcg cgagaaatct gcgatctacc 1080 gttggagga ggagtatgaa aacctgctga aagcgtcctt tgagaggatg gatcacctgc 1140 acagctgca gaacatcatt caggccacgt ccagggagat catgtggatc aatgactgcg 1200 ggaggagga gctgctgtac gactggagcg acaagaacac caacatcgct cagaaacagg 1260 ggccttctc catacgcatg agtcaactgg aagttaaaga aaaagagctc aataagctga 1320 acaagaaag tgaccaactt gtcctcaatc agcatccagc ttcagacaaa attgaggcct 1380 tatggacac tctgcagacg cagtggagtt ggattcttca gatcaccaag tgcattgatg 1440 tcatctgaa agaaaatgct gcctactttc agttttttga agaggcgcag tctactgaag 1500 atacctgaa ggggctccag gactccatca ggaagaagta cccctgcgac aagaacatgc 1560 cctgcagca cctgctggaa cagatcaagg agctggagaa agaacgagag aaaatccttg 1620 atacaagcg tcaggtgcag aacttggtaa acaagtctaa gaagattgta cagctgaagc 1680 tcgtaaccc agactacaga agcaataaac ccattattct cagagctctc tgtgactaca 1740 acaagatca gaaaatcgtg cataaggggg atgagtgtat cctgaaggac aacaacgagc 1800 cagcaagtg gtacgtgacg ggcccgggag gcgttgacat gcttgttccc tctgtggggc 1860 gatcatccc tcctccgaac ccactggccg tggacctctc ttgcaagatt gagcagtact 1920 cgaagccat cttggctctg tggaaccagc tctacatcaa catgaagagc ctggtgtcct 1980 gcactactg catgattgac atagagaaga tcagggccat gacaatcgcc aagctgaaaa 2040 aatgcggca ggaagattac atgaagacga tagccgacct tgagttacat taccaagagt 2100 catcagaaa tagccaaggc tcagagatgt ttggagatga tgacaagcgg aaaatacagt 2160 tcagttcac cgatgcccag aagcattacc agaccctggt cattcagctc cctggctatc 2220 ccagcacca gacagtgacc acaactgaaa tcactcatca tggaacctgc caagatgtca 2280 ccataataa agtaattgaa accaacagag aaaatgacaa gcaagaaaca tggatgctga 2340 ggagctgca gaagattcgc aggcagatag agcactgcga gggcaggatg actctcaaaa 2400 cctccctct agcagaccag gggtcttctc accacatcac agtgaaaatt aacgagctta 2460 gagtgtgca gaatgattca caagcaattg ctgaggttct caaccagctt aaagatatgc 2520 tgccaactt cagaggttct gaaaagtact gctatttaca gaatgaagta tttggactat 2580 tcagaaact ggaaaatatc aatggtgtta cagatggcta cttaaatagc ttatgcacag 2640 aagggcact gctccaggct attctccaaa cagaagacat gttaaaggtt tatgaagcca 2700 gctcactga ggaggaaact gtctgcctgg acctggataa agtggaagct taccgctgtg 2760 actgaagaa aataaaaaat gacttgaact tgaagaagtc gttgttggcc actatgaaga 2820 agaactaca gaaagcccag cagatccact ctcagacttc acagcagtat ccactttatg 2880 tctggactt gggcaagttc ggtgaaaaag tcacacagct gacagaccgc tggcaaagga 2940 agataaaca gatcgacttt agattatggg acctggagaa acaaatcaag caattgagga 3000 ttatcgtga taactatcag gctttctgca agtggctcta tgatcgtaaa cgccgccagg 3060 ttccttaga atccatgaaa tttggagatt ccaacacagt catgcggttt ttgaatgagc 3120 gaagaactt gcacagtgaa atatctggca aacgagacaa atcagaggaa gtacaaaaaa 3180 tgctgaact ttgcgccaat tcaattaagg attatgagct ccagctggcc tcatacacct 3240 aggactgga aactctgctg aacataccta tcaagaggac catgattcag tccccttctg 3300 ggtgattct gcaagaggct gcagatgttc atgctcggta cattgaacta cttacaagat 3360 tggagacta ttacaggttc ttaagtgaga tgctgaagag tttggaagat ctgaagctga 3420 aaataccaa gatcgaagtt ttggaagagg agctcagact ggcccgagat gccaactcgg 3480 aaactgtaa taagaacaaa ttcctggatc agaacctgca gaaataccag gcagagtgtt 3540 ccagttcaa agcgaagctt gcgagcctgg aggagctgaa gagacaggct gagctggatg 3600 gaagtcggc taagcaaaat ctagacaagt gctacggcca aataaaagaa ctcaatgaga 3660 gatcacccg actgacttat gagattgaag atgaaaagag aagaagaaaa tctgtggaag 3720 cagatttga ccaacagaag aatgactatg accaactgca gaaagcaagg caatgtgaaa 3780 ggagaacct tggttggcag aaattagagt ctgagaaagc catcaaggag aaggagtacg 3840 gattgaaag gttgagggtt ctactgcagg aagaaggcac ccggaagaga gaatatgaaa 3900 tgagctggc aaaggtaaga aaccactata atgaggagat gagtaattta aggaacaagt 3960 tgaaacaga gattaacatt acgaagacca ccatcaagga gatatccatg caaaaagagg 4020 tgattccaa aaatcttaga aaccagcttg atagactttc aagggaaaat cgagatctga 4080 ggatgaaat tgtcaggctc aatgacagca tcttgcaggc cactgagcag cgaaggcgag 4140 tgaagaaaa cgcccttcag caaaaggcct gtggctctga gataatgcag aagaagcagc 4200 tctggagat agaactgaag caggtcatgc agcagcgctc tgaggacaat gcccggcaca 4260 gcagtccct ggaggaggct gccaagacca ttcaggacaa aaataaggag atcgagagac 4320 caaagctga gtttcaggag gaggccaagc gccgctggga atatgaaaat gaactgagta 4380 ggtaagaaa caattatgat gaggagatca ttagcttaaa aaatcagttt gagaccgaga 4440 caacatcac caagaccacc atccaccagc tcaccatgca gaaggaagag gataccagtg 4500 ctaccgggc tcagatagac aatctcaccc gagaaaacag gagcttatct gaagaaataa 4560 gaggctgaa gaacactcta acccagacca cagagaatct caggagggtg gaagaagaca 4620 ccaacagca aaaggccact ggctctgagg tgtctcagag gaaacagcag ctggaggttg 4680 gctgagaca agtcactcag atgcgaacag aggagagcgt aagatataag caatctcttg 4740 tgatgctgc caaaaccatc caggataaaa acaaggagat agaaaggtta aaacaactga 4800 cgacaaaga aacaaatgac cggaaatgcc tggaagatga aaacgcgaga ttacaaaggg 4860 ccagtatga cctgcagaaa gcaaacagta gtgcgacgga gacaataaac aaactgaagg 4920 tcaggagca agaactgaca cgcctgagga tcgactatga aagggtttcc caggagagga 4980 tgtgaagga ccaggatatc acgcggttcc agaactctct gaaagagctg cagctgcaga 5040 gcagaaggt ggaagaggag ctgaatcggc tgaagaggac cgcgtcagaa gactcctgca 5100 gaggaagaa gctggaggaa gagctggaag gcatgaggag gtcgctgaag gagcaagcca 5160 caaaatcac caacctgacc cagcagctgg agcaggcatc cattgttaag aagaggagtg 5220 ggatgacct ccggcagcag agggacgtgc tggatggcca cctgagggaa aagcagagga 5280 ccaggaaga gctgaggagg ctctcttctg aggtcgaggc cctgaggcgg cagttactcc 5340 ggaacagga aagtgtcaaa caagctcact tgaggaatga gcatttccag aaggcgatag 5400 agataaaag cagaagctta aatgaaagca aaatagaaat tgagaggctg cagtctctca 5460 agagaacct gaccaaggag cacttgatgt tagaagaaga actgcggaac ctgaggctgg 5520 gtacgatga cctgaggaga ggacgaagcg aagcggacag tgataaaaat gcaaccatct 5580 ggaactaag gagccagctg cagatcagca acaaccggac cctggaactg caggggctga 5640 taatgattt acagagagag agggaaaatt tgagacagga aattgagaaa ttccaaaagc 5700 ggctttaga ggcatctaat aggattcagg aatcaaagaa tcagtgtact caggtggtac 5760 ggaaagaga gagccttctg gtgaaaatca aagtcctgga gcaagacaag gcaaggctgc 5820 gaggctgga ggatgagctg aatcgtgcaa aatcaactct agaggcagaa accagggtga 5880 acagcgcct ggagtgtgag aaacagcaaa ttcagaatga cctgaatcag tggaagactc 5940 atattcccg caaggaggag gctattagga agatagaatc ggaaagagaa aagagtgaga 6000 agagaagaa cagtcttagg agtgagatcg aaagactcca agcagagatc aagagaattg 6060 agagaggtg caggcgtaag ctggaggatt ctaccaggga gacacagtca cagttagaaa 6120 agaacgctc ccgatatcag agggagattg ataaactcag acagcgccca tatgggtccc 6180 tcgagagac ccagactgag tgtgagtgga ccgttgacac ctccaagctg gtgtttgatg 6240 gctgaggaa gaaggtgaca gcaatgcagc tctatgagtg tcagctgatc gacaaaacaa 6300 cttggacaa actattgaag gggaagaagt cagtggaaga agttgcttct gaaatccagc 6360 attccttcg gggtgcagga tctatcgctg gagcatctgc ttctcctaag gaaaaatact 6420 tttggtaga ggccaagaga aagaaattaa tcagcccaga atccacagtc atgcttctgg 6480 ggcccaggc agctacaggt ggtataattg atccccatcg gaatgagaag ctgactgtcg 6540 cagtgccat agctcgggac ctcattgact tcgatgaccg tcagcagata tatgcagcag 6600 aaaagctat cactggtttt gatgatccat tttcaggcaa gacagtatct gtttcagaag 6660 catcaagaa aaatttgatt gatagagaaa ccggaatgcg cctgctggaa gcccagattg 6720 ttcaggggg tgtagtagac cctgtgaaca gtgtcttttt gccaaaagat gtcgccttgg 6780 ccgggggct gattgataga gatttgtatc gatccctgaa tgatccccga gatagtcaga 6840 aaactttgt ggatccagtc accaaaaaga aggtcagtta cgtgcagctg aaggaacggt 6900 cagaatcga accacatact ggtctgctct tgctttcagt acagaagaga agcatgtcct 6960 ccaaggaat cagacaacct gtgaccgtca ctgagctagt agattctggt atattgagac 7020 gtccactgt caatgaactg gaatctggtc agatttctta tgacgaggtt ggtgagagaa 7080 taaggactt cctccagggt tcaagctgca tagcaggcat atacaatgag accacaaaac 7140 gaagcttgg catttatgag gccatgaaaa ttggcttagt ccgacctggt actgctctgg 7200 gttgctgga agcccaagca gctactggct ttatagtgga tcctgttagc aacttgaggt 7260 accagtgga ggaagcctac aagagaggtc tggtgggcat tgagttcaaa gagaagctcc 7320 gtctgcaga acgagctgtc actgggtata atgatcctga aacaggaaac atcatctctt 7380 gttccaagc catgaataag gaactcatcg aaaagggcca cggtattcgc ttattagaag 7440 acagatcgc aaccgggggg atcattgacc caaaggagag ccatcgttta ccagttgaca 7500 agcatataa gaggggctat ttcaatgagg aactcagtga gattctctca gatccaagtg 7560 tgataccaa aggatttttt gaccccaaca ctgaagaaaa tcttacctat ctgcaactaa 7620 agaaagatg cattaaggat gaggaaacag ggctctgtct tctgcctctg aaagaaaaga 7680 gaaacaggt gcagacatca caaaagaata ccctcaggaa gcgtagagtg gtcatagttg 7740 cccagaaac caataaagaa atgtctgttc aggaggccta caagaagggc ctaattgatt 7800 tgaaacctt caaagaactg tgtgagcagg aatgtgaatg ggaagaaata accatcacgg 7860 atcagatgg ctccaccagg gtggtcctgg tagatagaaa gacaggcagt cagtatgata 7920 tcaagatgc tattgacaag ggccttgttg acaggaagtt ctttgatcag taccgatccg 7980 cagcctcag cctcactcaa tttgctgaca tgatctcctt gaaaaatggt gtcggcacca 8040 cagcagcat gggcagtggt gtcagcgatg atgtttttag cagctcccga catgaatcag 8100 aagtaagat ttccaccata tccagcgtca ggaatttaac cataaggagc agctcttttt 8160 agacaccct ggaagaatcg agccccattg cagccatctt tgacacagaa aacctggaga 8220 aatctccat tacagaaggt atagagcggg gcatcgttga cagcatcacg ggtcagaggc 8280 tctggaggc tcaggcctgc acaggtggca tcatccaccc aaccacgggc cagaagctgt 8340 acttcagga cgcagtctcc cagggtgtga ttgaccaaga catggccacc agcgtgaagc 8400 tgctcagaa agccttcata ggcttcgagg gtgtgaaggg aaagaagaag atgtcagcag 8460 agaggcagt gaaagaaaaa tggctcccgt atgaggctgg ccagcgcttc ctggagttcc 8520 gtacctcac gggaggtctt gttgacccgg aagtgcatgg gaggataagc accgaagaag 8580 catccggaa ggggttcata gatggccgcg ccgcacagag gctgcaagac accagcagct 8640 tgccaaaat cctgacctgc cccaaaacca aattaaaaat atcctataag gatgccataa 8700 tcgctccat ggtagaagat atcactgggc tgcgccttct ggaagccgcc tccgtgtcgt 8760 caagggctt acccagccct tacaacatgt cttcggctcc ggggtcccgc tccggctccc 8820 ctcgggatc tcgctccgga tctcgctccg ggtcccgcag tgggtcccgg agaggaagct 8880 tgacgccac agggaattct tcctactctt attcctactc atttagcagt agttctattg 8940 gcactag 8948 120 587 DNA Homo sapien misc_feature (1)...(587) n = A,T,C or G 120 cgtcctaagc acttagacta catcagggaa gaacacagac cacatccctg tcctcatgcg 60 gcttatgttt tctggaagaa agtggagacc nagtccttgg ctttagggct ccccggctgg 120 gggctgtgca ntccggtcag ggcgggaagg gaaatgcacc gctgcatgtg aacttacagc 180 ccaggcggat gccccttccc ttagcactac ctggcctcct gcatcccctc gcctcatgtt 240 cctcccacct tcaaanaatg aanaacccca tgggcccagc cccttgccct ggggaaccaa 300 ggcagccttc caaaactcag gggctgaagc anactattag ggcaggggct gactttgggt 360 gacactgccc attccctctc agggcagctc angtcacccn ggnctcttga acccagcctg 420 ttcctttgaa aaagggcaaa actgaaaagg gcttttccta naaaaagaaa aaccagggaa 480 ctttgccagg gcttcnntnt taccaaaacn ncttctcnng gatttttaat tccccattng 540 gcctccactt accnggggcn atgccccaaa attaanaatt tcccatc 587 121 619 DNA Homo sapien misc_feature (1)...(619) n = A,T,C or G 121 cactagtagg atagaaacac tgtgtcccga gagtaaggag agaagctact attgattaga 60 gcctaaccca ggttaactgc aagaagaggc gggatacttt cagctttcca tgtaactgta 120 tgcataaagc caatgtagtc cagtttctaa gatcatgttc caagctaact gaatcccact 180 tcaatacaca ctcatgaact cctgatggaa caataacagg cccaagcctg tggtatgatg 240 tgcacacttg ctagactcan aaaaaatact actctcataa atgggtggga gtattttggt 300 gacaacctac tttgcttggc tgagtgaagg aatgatattc atatattcat ttattccatg 360 gacatttagt tagtgctttt tatataccag gcatgatgct gagtgacact cttgtgtata 420 tttccaaatt tttgtacagt cgctgcacat atttgaaatc atatattaag acttccaaaa 480 aatgaagtcc ctggtttttc atggcaactt gatcagtaaa ggattcncct ctgtttggta 540 cttaaaacat ctactatatn gttnanatga aattcctttt ccccncctcc cgaaaaaana 600 aagtggtggg gaaaaaaaa 619 122 1475 DNA Homo sapien 122 tccacctgtc cccgcagcgc cggctcgcgc cctcctgccg cagccaccga gccgccgtct 60 agcgccccga cctcgccacc atgagagccc tgctggcgcg cctgcttctc tgcgtcctgg 120 tcgtgagcga ctccaaaggc agcaatgaac ttcatcaagt tccatcgaac tgtgactgtc 180 taaatggagg aacatgtgtg tccaacaagt acttctccaa cattcactgg tgcaactgcc 240 caaagaaatt cggagggcag cactgtgaaa tagataagtc aaaaacctgc tatgagggga 300 atggtcactt ttaccgagga aaggccagca ctgacaccat gggccggccc tgcctgccct 360 ggaactctgc cactgtcctt cagcaaacgt accatgccca cagatctgat gctcttcagc 420 tgggcctggg gaaacataat tactgcagga acccagacaa ccggaggcga ccctggtgct 480 atgtgcaggt gggcctaaag ccgcttgtcc aagagtgcat ggtgcatgac tgcgcagatg 540 gaaaaaagcc ctcctctcct ccagaagaat taaaatttca gtgtggccaa aagactctga 600 ggccccgctt taagattatt gggggagaat tcaccaccat cgagaaccag ccctggtttg 660 cggccatcta caggaggcac cgggggggct ctgtcaccta cgtgtgtgga ggcagcctca 720 tcagcccttg ctgggtgatc agcgccacac actgcttcat tgattaccca aagaaggagg 780 actacatcgt ctacctgggt cgctcaaggc ttaactccaa cacgcaaggg gagatgaagt 840 ttgaggtgga aaacctcatc ctacacaagg actacagcgc tgacacgctt gctcaccaca 900 acgacattgc cttgctgaag atccgttcca aggagggcag gtgtgcgcag ccatcccgga 960 ctatacagac catctgcctg ccctcgatgt ataacgatcc ccagtttggc acaagctgtg 1020 agatcactgg ctttggaaaa gagaattcta ccgactatct ctatccggag cagctgaaga 1080 tgactgttgt gaagctgatt tcccaccggg agtgtcagca gccccactac tacggctctg 1140 aagtcaccac caaaatgctg tgtgctgctg acccacagtg gaaaacagat tcctgccagg 1200 gagactcagg gggacccctc gtctgttccc tccaaggccg catgactttg actggaattg 1260 tgagctgggg ccgtggatgt gccctgaagg acaagccagg cgtctacacg agagtctcac 1320 acttcttacc ctggatccgc agtcacacca aggaagagaa tggcctggcc ctctgagggt 1380 ccccagggag gaaacgggca ccacccgctt tcttgctggt tgtcattttt gcagtagagt 1440 catctccatc agctgtaaga agagactggg aagat 1475 123 2294 DNA Homo sapien 123 cagcgccggc tcgcgccctc ctgccgcagc caccgagccg ccgtctagcg ccccgacctc 60 gccaccatga gagccctgct ggcgcgcctg cttctctgcg tcctggtcgt gagcgactcc 120 aaaggcagca atgaacttca tcaagttcca tcgaactgtg actgtctaaa tggaggaaca 180 tgtgtgtcca acaagtactt ctccaacatt cactggtgca actgcccaaa gaaattcgga 240 gggcagcact gtgaaataga taagtcaaaa acctgctatg aggggaatgg tcacttttac 300 cgaggaaagg ccagcactga caccatgggc cggccctgcc tgccctggaa ctctgccact 360 gtccttcagc aaacgtacca tgcccacaga tctgatgctc ttcagctggg cctggggaaa 420 cataattact gcaggaaccc agacaaccgg aggcgaccct ggtgctatgt gcaggtgggc 480 ctaaagccgc ttgtccaaga gtgcatggtg catgactgcg cagatggaaa aaagccctcc 540 tctcctccag aagaattaaa atttcagtgt ggccaaaaga ctctgaggcc ccgctttaag 600 attattgggg gagaattcac caccatcgag aaccagccct ggtttgcggc catctacagg 660 aggcaccggg ggggctctgt cacctacgtg tgtggaggca gcctcatcag cccttgctgg 720 gtgatcagcg ccacacactg cttcattgat tacccaaaga aggaggacta catcgtctac 780 ctgggtcgct caaggcttaa ctccaacacg caaggggaga tgaagtttga ggtggaaaac 840 ctaatcctac acaaggacta cagcgctgac acgcttgctc accacaacga cattgccttg 900 ctgaagatcc gttccaagga gggcaggtgt gcgcagccat cccggactat acagaccatc 960 tgcctgccct cgatgtataa cgatccccag tttggcacaa gctgtgagat cactggcttt 1020 ggaaaagaga attctaccga ctatctctat ccggagcagc tgaaaatgac tgttgtgaag 1080 ctgatttccc accgggagtg tcagcagccc cactactacg gctctgaagt caccaccaaa 1140 atgctgtgtg ctgctgaccc acagtggaaa acagattcct gccagggaga ctcaggggga 1200 cccctcgtct gttccctcca aggccgcatg actttgactg gaattgtgag ctggggccgt 1260 ggatgtgccc tgaaggacaa gccaggcgtc tacacgagag tctcacactt cttaccctgg 1320 atccgcagtc acaccaagga agagaatggc ctggccctct gagggtcccc agggaggaaa 1380 cgggcaccac ccgctttctt gctggttgct attttgcagt agagtcatct ccatcagctg 1440 taagaagagc tgggaatata ggctctgcac agatggattt gcctgtgcca ccaccagggc 1500 gaacgacaat agctttaccc tcaggcatag gcctgggtgc tggctgccca gacccctctg 1560 gccaggatgg aggggtggtc ctgactcaac atgttactga ccagcaactt gtctttttct 1620 ggactgaagc ctgcaggagt taaaaagggc agggcatctc ctgtgcatgg gctcgaaggg 1680 agagccagct cccccgaccg gtgggcattt gtgaggccca tggttgagaa atgaataatt 1740 tcccaattag gaagtgtaag cagctgaggt ctcttgaggg agcttagcca atgtgggagc 1800 agcggtttgg ggagcagaga cactaacgac ttcagggcag ggctctgata ttccatgaat 1860 gtatcaggaa atatatatgt gtgtgtatgt ttgcacactt gtgtgtgggc tgtgagtgta 1920 agtgtgagta agagctggtg tctgattgtt aagtctaaat atttccttaa actgtgtgga 1980 ctgtgatgcc acacagagtg gtctttctgg agaggttata ggtcactcct ggggcctctt 2040 gggtccccca cgtgacagtg cctgggaatg tattattctg cagcatgacc tgtgaccagc 2100 actgtctcag tttcactttc acatagatgt ccctttcttg gccagttatc ccttcctttt 2160 agcctagttc atccaatcct cactgggtgg ggtgaggacc actcctgtac actgaatatt 2220 tatatttcac tatttttatt tatatttttg taattttaaa taaaagtgat caataaaatg 2280 tgatttttct gatg 2294 124 956 DNA Homo sapien 124 gatgagttcc gcaccaagtt tgagacagac caggccctgc gcctgagtgt ggaggccgac 60 atcaatggcc tgcgcagggt gctggatgag ctgaccctgg ccagagccga cctggagatg 120 cagattgaga acctcaagga ggagctggcc tacctgaaga agaaccacga ggaggagatg 180 aacgccctgc gaggccaggt gggtggtgag atcaatgtgg agatggacgc tgccccaggc 240 gtggacctga gccgcatcct caacgagatg cgtgaccagt atgagaagat ggcagagaag 300 aaccgcaagg atgccgagga ttggttcttc agcaagacag aggaactgaa ccgcgaggtg 360 gccaccaaca gtgagctggt gcagagtggc aagagtgaga tctcggagct ccggcgcacc 420 atgcaggcct tggagataga gctgcagtcc cagctcagca tgaaagcatc cctggagggc 480 aacctggcgg agacagagaa ccgctactgc gtgcagctgt cccagatcca ggggctgatt 540 ggcagcgtgg aggagcagct ggcccagctt cgctgcgaga tggagcagca gaaccaggaa 600 tacaaaatcc tgctggatgt gaagacgcgg ctggagcagg agattgccac ctaccgccgc 660 ctgctggagg gagaggatgc ccacctgact cagtacaaga aagaaccggt gaccacccgt 720 caggtgcgta ccattgtgga agaggtccag gatggcaagg tcatctcctc ccgcgagcag 780 gtccaccaga ccacccgctg aggactcagc taccccggcc ggccacccag gaggcaggga 840 cgcagccgcc ccatctgccc cacagtctcc ggcctctcca gcctcagccc cctgcttcag 900 tcccttcccc atgcttcctt gcctgatgac aataaaagct tgttgactca gctatg 956 125 486 DNA Homo sapien misc_feature (1)...(486) n = A,T,C or G 125 aaattatata tagtgnttca gctcccattg tggtgttcat agtcttctag gaacagataa 60 acttaagtat tcaattcact cttggcattt tttctttaat ataggctttt tagcctattt 120 ttggaaaact gcttttcttc tgagaacctt attctgaatg tcatcaactt taccaaacct 180 tctaagtcca gagctaactt agtactgttt aagttactat tgactgaatt ttcttcattt 240 tctgtttagc cagtgttacc aaggtaagct ggggaatgaa gtataccaac ttctttcaga 300 gcattttagg acattatggc agctttagaa ggctgtcttg tttctagcca agggagagcc 360 agcgcaggtt ttggatacta gagaaagtca tttgcttgta ctattgccat tttagaaagc 420 tctgatgtga attcaaattt tacctctgtt acttaaagcc aacaatttta aggcagtagt 480 tttact 486 126 3552 DNA Homo sapien 126 cggcaggcag gtctcgtctc ggcaccctcc cggcgcccgc gttctcctgg ccctgcccgg 60 catcccgatg gccgccgctg ggccccggcg ctccgtgcgc ggagccgtct gcctgcatct 120 gctgctgacc ctcgtgatct tcagtcgtgc tggtgaagcc tgcaaaaagg tgatacttaa 180 tgtaccttct aaactagagg cagacaaaat aattggcaga gttaatttgg aagagtgctt 240 caggtctgca gacctcatcc ggtcaagtga tcctgatttc agagttctaa atgatgggtc 300 agtgtacaca gccagggctg ttgcgctgtc tgataagaaa agatcattta ccatatggct 360 ttctgacaaa aggaaacaga cacagaaaga ggttactgtg ctgctagaac atcagaagaa 420 ggtatcgaag acaagacaca ctagagaaac tgttctcagg cgtgccaaga ggagatgggc 480 acctattcct tgctctatgc aagagaattc cttgggccct ttcccattgt ttcttcaaca 540 agttgaatct gatgcagcac agaactatac tgtcttctac tcaataagtg gacgtggagt 600 tgataaagaa cctttaaatt tgttttatat agaaagagac actggaaatc tattttgcac 660 tcggcctgtg gatcgtgaag aatatgatgt ttttgatttg attgcttatg cgtcaactgc 720 agatggatat tcagcagatc tgcccctccc actacccatc agggtagagg atgaaaatga 780 caaccaccct gttttcacag aagcaattta taattttgaa gttttggaaa gtagtagacc 840 tggtactaca gtgggggtgg tttgtgccac agacagagat gaaccggaca caatgcatac 900 gcgcctgaaa tacagcattt tgcagcagac accaaggtca cctgggctct tttctgtgca 960 tcccagcaca ggcgtaatca ccacagtctc tcattatttg gacagagagg ttgtagacaa 1020 gtactcattg ataatgaaag tacaagacat ggatggccag ttttttggat tgataggcac 1080 atcaacttgt atcataacag taacagattc aaatgataat gcacccactt tcagacaaaa 1140 tgcttatgaa gcatttgtag aggaaaatgc attcaatgtg gaaatcttac gaatacctat 1200 agaagataag gatttaatta acactgccaa ttggagagtc aattttacca ttttaaaggg 1260 aaatgaaaat ggacatttca aaatcagcac agacaaagaa actaatgaag gtgttctttc 1320 tgttgtaaag ccactgaatt atgaagaaaa ccgtcaagtg aacctggaaa ttggagtaaa 1380 caatgaagcg ccatttgcta gagatattcc cagagtgaca gccttgaaca gagccttggt 1440 tacagttcat gtgagggatc tggatgaggg gcctgaatgc actcctgcag cccaatatgt 1500 gcggattaaa gaaaacttag cagtggggtc aaagatcaac ggctataagg catatgaccc 1560 cgaaaataga aatggcaatg gtttaaggta caaaaaattg catgatccta aaggttggat 1620 caccattgat gaaatttcag ggtcaatcat aacttccaaa atcctggata gggaggttga 1680 aactcccaaa aatgagttgt ataatattac agtcctggca atagacaaag atgatagatc 1740 atgtactgga acacttgctg tgaacattga agatgtaaat gataatccac cagaaatact 1800 tcaagaatat gtagtcattt gcaaaccaaa aatggggtat accgacattt tagctgttga 1860 tcctgatgaa cctgtccatg gagctccatt ttatttcagt ttgcccaata cttctccaga 1920 aatcagtaga ctgtggagcc tcaccaaagt taatgataca gctgcccgtc tttcatatca 1980 gaaaaatgct ggatttcaag aatataccat tcctattact gtaaaagaca gggccggcca 2040 agctgcaaca aaattattga gagttaatct gtgtgaatgt actcatccaa ctcagtgtcg 2100 tgcgacttca aggagtacag gagtaatact tggaaaatgg gcaatccttg caatattact 2160 gggtatagca ctgctctttt ctgtattgct aactttagta tgtggagttt ttggtgcaac 2220 taaagggaaa cgttttcctg aagatttagc acagcaaaac ttaattatat caaacacaga 2280 agcacctgga gacgatagag tgtgctctgc caatggattt atgacccaaa ctaccaacaa 2340 ctctagccaa ggtttttgtg gtactatggg atcaggaatg aaaaatggag ggcaggaaac 2400 cattgaaatg atgaaaggag gaaaccagac cttggaatcc tgccgggggg ctgggcatca 2460 tcataccctg gactcctgca ggggaggaca cacggaggtg gacaactgca gatacactta 2520 ctcggagtgg cacagtttta ctcaaccccg tctcggtgaa aaattgcatc gatgtaatca 2580 gaatgaagac cgcatgccat cccaagatta tgtcctcact tataactatg agggaagagg 2640 atctccagct ggttctgtgg gctgctgcag tgaaaagcag gaagaagatg gccttgactt 2700 tttaaataat ttggaaccca aatttattac attagcagaa gcatgcacaa agagataatg 2760 tcacagtgct acaattaggt ctttgtcaga cattctggag gtttccaaaa ataatattgt 2820 aaagttcaat ttcaacatgt atgtatatga tgattttttt ctcaattttg aattatgcta 2880 ctcaccaatt tatattttta aagcaagttg ttgcttatct tttccaaaaa gtgaaaaatg 2940 ttaaaacaga caactggtaa atctcaaact ccagcactgg aattaaggtc tctaaagcat 3000 ctgctctttt ttttttttac agatatttta gtaataaata tgctggataa atattagtcc 3060 aacaatagct aagttatgct aatatcacat tattatgtat tcactttaag tgatagttta 3120 aaaaataaac aagaaatatt gagtatcact atgtgaagaa agttttggaa aagaaacaat 3180 gaagactgaa ttaaattaaa aatgttgcag ctcataaaga attggactca cccctactgc 3240 actaccaaat tcatttgact ttggaggcaa aatgtgttga agtgccctat gaagtagcaa 3300 ttttctatag gaatatagtt ggaaataaat gtgtgtgtgt atattattat taatcaatgc 3360 aatatttaaa tgaaatgaga acaaagagga aaatggtaaa aacttgaaat gaggctgggg 3420 tatagtttgt cctacaatag aaaaaagaga gagcttccta ggcctgggct cttaaatgct 3480 gcattataac tgagtctatg aggaaatagt tcctgtccaa tttgtgtaat ttgtttaaaa 3540 ttgtaaataa at 3552 127 754 DNA Homo sapien 127 tttttttttt ttgtcattgt tcattgattt taatgagaaa gctaagagag gaaataagta 60 gcctttcaaa ggtcacacag aagtaagtga cagatccagg attcatatcc aagcattctg 120 gctctagtgt ccatgcttct caaccattat gacccaatat tcaaccaaat caatactgaa 180 ggacacgtga aatgtatccg gtattttact attacaaaca aaaatccaat gaacattctt 240 gaagacatac acaaaaataa tggttacaat agaagttact ggaattgaaa ttttggttca 300 acctatatta aaatgtaagg cttttgatat agctaataga tttttgaaat gatcagtctt 360 aacgtttgta ggggagcaca ctcctgcatg gggaaaagat tcactgtgaa gcacagagca 420 cctttatggt tggatcatct tgtcattaaa gttcaggcgt tatctatcct gtaagtggca 480 gaatcaagac tgcaatatcg cctgcttttc tttttaactc atgttttccc ttgactacac 540 tggtcctcaa agtaaaaccc ctgtgtcagt gtactattca tggaatactc tgcaattata 600 accaccttct aatactttta atacccaatc aaaatttatt atacatatgt atcatagata 660 ctcatctgta aagctgtgct tcaaaatagt gatctcttcc caacattaca atatatatta 720 atgatgtcga acctgcccgg gcggccgctc gaag 754 128 374 DNA Homo sapien 128 aggttttgat taaaaaggca aatgatttta ttgttcgata atcttttaaa aaaataagag 60 gaaggagtaa aattaaagat gaaagatgat ttttatttcc ttgtgacctc tatatccccc 120 ttcccctgcc cttggtaagt aactcttgat ggagaaagga ttaaagactc ttatttaacc 180 aaaaaacaga gccagctaat catttccaaa ggttagtatc tccctgctga cctcttcttt 240 ggtttaattg aataaaacta tatgttcata tatgtattaa aacaactcag aataacatct 300 tttcttcctt agttaaggca ttataagggc tatactatca tccataataa ccaaggcaat 360 aacttaaaaa gctg 374 129 546 DNA Homo sapien 129 agtgtgatgg atatctgcag aattcgggct aagcgtggtc gcggcccgag gtctggaact 60 tcccagcacy tgaaaaggag cctcctgagc tgactcggct aaagccccac tttcgctcct 120 cctcatttct gcctactgat ttccttggag cattcatctg aatattaccg tttgctgtgt 180 aacctggtac atacatagca tgactccctg gaatagagtg ggctggggtg cttatgctgg 240 gagagtgatt gacatgcact ttcaagctat atctaccatt tgcagcaaag gagaaaaaat 300 acctcgagta aattccatca ttttttataa catcagcacc tgctccatca tcaaggagtc 360 tcagcgtaac aggatctcca gtctctggct caactgtggc agtgacagtg gcattaagaa 420 tgggataaaa tccctgtttc acattggcat aaatcatcac aggatgagga aaatggaggc 480 tgtctctttc cacaaaggct tccacagtgg ctgggggcac agacctgccc gggcggccgc 540 tcgaaa 546 130 5156 DNA Homo sapien 130 ccaaccgag gcgccgggca gcgacccctg cagcggagac agagactgag cggcccggca 60 cgccatgcc tgcgctctgg ctgggctgct gcctctgctt gtcgctcctc ctgcccgcag 120 ccgggccac ctccaggagg gaagtctgtg attgcaatgg gaagtccagg cagtgtatct 180 tgatcggga acttcacaga caaactggta atggattccg ctgcctcaac tgcaatgaca 240 cactgatgg cattcactgc gagaagtgca agaatggctt ttaccggcac agagaaaggg 300 ccgctgttt gccctgcaat tgtaactcca aaggttctct tagtgctcga tgtgacaact 360 cggacggtg cagctgtaaa ccaggtgtga caggagccag atgcgaccga tgtctgccag 420 cttccacat gctcacggat gcggggtgca cccaagacca gagactgcta gactccaagt 480 tgactgtga cccagctggc atcgcagggc cctgtgacgc gggccgctgt gtctgcaagc 540 agctgtcac tggagaacgc tgtgataggt gtcgatcagg ttactataat ctggatgggg 600 gaaccctga gggctgtacc cagtgtttct gctatgggca ttcagccagc tgccgcagct 660 tgcagaata cagtgtccat aagatcacct ctacctttca tcaagatgtt gatggctgga 720 ggctgtcca acgaaatggg tctcctgcaa agctccaatg gtcacagcgc catcaagatg 780 gtttagctc agcccaacga ctagaccctg tctattttgt ggctcctgcc aaatttcttg 840 gaatcaaca ggtgagctat ggtcaaagcc tgtcctttga ctaccgtgtg gacagaggag 900 cagacaccc atctgcccat gatgtgattc tggaaggtgc tggtctacgg atcacagctc 960 cttgatgcc acttggcaag acactgcctt gtgggctcac caagacttac acattcaggt 1020 aaatgagca tccaagcaat aattggagcc cccagctgag ttactttgag tatcgaaggt 1080 actgcggaa tctcacagcc ctccgcatcc gagctacata tggagaatac agtactgggt 1140 cattgacaa tgtgaccctg atttcagccc gccctgtctc tggagcccca gcaccctggg 1200 tgaacagtg tatatgtcct gttgggtaca aggggcaatt ctgccaggat tgtgcttctg 1260 ctacaagag agattcagcg agactggggc cttttggcac ctgtattcct tgtaactgtc 1320 agggggagg ggcctgtgat ccagacacag gagattgtta ttcaggggat gagaatcctg 1380 cattgagtg tgctgactgc ccaattggtt tctacaacga tccgcacgac ccccgcagct 1440 caagccatg tccctgtcat aacgggttca gctgctcagt gatgccggag acggaggagg 1500 ggtgtgcaa taactgccct cccggggtca ccggtgcccg ctgtgagctc tgtgctgatg 1560 ctactttgg ggaccccttt ggtgaacatg gcccagtgag gccttgtcag ccctgtcaat 1620 caacaacaa tgtggacccc agtgcctctg ggaattgtga ccggctgaca ggcaggtgtt 1680 gaagtgtat ccacaacaca gccggcatct actgcgacca gtgcaaagca ggctacttcg 1740 ggacccatt ggctcccaac ccagcagaca agtgtcgagc ttgcaactgt aaccccatgg 1800 ctcagagcc tgtaggatgt cgaagtgatg gcacctgtgt ttgcaagcca ggatttggtg 1860 ccccaactg tgagcatgga gcattcagct gtccagcttg ctataatcaa gtgaagattc 1920 gatggatca gtttatgcag cagcttcaga gaatggaggc cctgatttca aaggctcagg 1980 tggtgatgg agtagtacct gatacagagc tggaaggcag gatgcagcag gctgagcagg 2040 ccttcagga cattctgaga gatgcccaga tttcagaagg tgctagcaga tcccttggtc 2100 ccagttggc caaggtgagg agccaagaga acagctacca gagccgcctg gatgacctca 2160 gatgactgt ggaaagagtt cgggctctgg gaagtcagta ccagaaccga gttcgggata 2220 tcacaggct catcactcag atgcagctga gcctggcaga aagtgaagct tccttgggaa 2280 cactaacat tcctgcctca gaccactacg tggggccaaa tggctttaaa agtctggctc 2340 ggaggccac aagattagca gaaagccacg ttgagtcagc cagtaacatg gagcaactga 2400 aagggaaac tgaggactat tccaaacaag ccctctcact ggtgcgcaag gccctgcatg 2460 aggagtcgg aagcggaagc ggtagcccgg acggtgctgt ggtgcaaggg cttgtggaaa 2520 attggagaa aaccaagtcc ctggcccagc agttgacaag ggaggccact caagcggaaa 2580 tgaagcaga taggtcttat cagcacagtc tccgcctcct ggattcagtg tctcggcttc 2640 gggagtcag tgatcagtcc tttcaggtgg aagaagcaaa gaggatcaaa caaaaagcgg 2700 ttcactctc aagcctggta accaggcata tggatgagtt caagcgtaca cagaagaatc 2760 gggaaactg gaaagaagaa gcacagcagc tcttacagaa tggaaaaagt gggagagaga 2820 atcagatca gctgctttcc cgtgccaatc ttgctaaaag cagagcacaa gaagcactga 2880 tatgggcaa tgccactttt tatgaagttg agagcatcct taaaaacctc agagagtttg 2940 cctgcaggt ggacaacaga aaagcagaag ctgaagaagc catgaagaga ctctcctaca 3000 cagccagaa ggtttcagat gccagtgaca agacccagca agcagaaaga gccctgggga 3060 cgctgctgc tgatgcacag agggcaaaga atggggccgg ggaggccctg gaaatctcca 3120 tgagattga acaggagatt gggagtctga acttggaagc caatgtgaca gcagatggag 3180 cttggccat ggaaaaggga ctggcctctc tgaagagtga gatgagggaa gtggaaggag 3240 gctggaaag gaaggagctg gagtttgaca cgaatatgga tgcagtacag atggtgatta 3300 agaagccca gaaggttgat accagagcca agaacgctgg ggttacaatc caagacacac 3360 caacacatt agacggcctc ctgcatctga tggaccagcc tctcagtgta gatgaagagg 3420 gctggtctt actggagcag aagctttccc gagccaagac ccagatcaac agccaactgc 3480 gcccatgat gtcagagctg gaagagaggg cacgtcagca gaggggccac ctccatttgc 3540 ggagacaag catagatggg attctggctg atgtgaagaa cttggagaac attagggaca 3600 cctgccccc aggctgctac aatacccagg ctcttgagca acagtgaagc tgccataaat 3660 tttctcaac tgaggttctt gggatacaga tctcagggct cgggagccat gtcatgtgag 3720 gggtgggat ggggacattt gaacatgttt aatgggtatg ctcaggtcaa ctgacctgac 3780 ccattcctg atcccatggc caggtggttg tcttattgca ccatactcct tgcttcctga 3840 gctgggcaa tgaggcagat agcactgggt gtgagaatga tcaaggatct ggaccccaaa 3900 aatagactg gatggaaaga caaactgcac aggcagatgt ttgcctcata atagtcgtaa 3960 tggagtcct ggaatttgga caagtgctgt tgggatatag tcaacttatt ctttgagtaa 4020 gtgactaaa ggaaaaaact ttgactttgc ccaggcatga aattcttcct aatgtcagaa 4080 agagtgcaa cccagtcaca ctgtggccag taaaatacta ttgcctcata ttgtcctctg 4140 aagcttctt gctgatcaga gttcctccta cttacaaccc agggtgtgaa catgttctcc 4200 ttttcaagc tggaagaagt gagcagtgtt ggagtgagga cctgtaaggc aggcccattc 4260 gagctatgg tgcttgctgg tgcctgccac cttcaagttc tggacctggg catgacatcc 4320 ttcttttaa tgatgccatg gcaacttaga gattgcattt ttattaaagc atttcctacc 4380 gcaaagcaa atgttgggaa agtatttact ttttcggttt caaagtgata gaaaagtgtg 4440 cttgggcat tgaaagaggt aaaattctct agatttatta gtcctaattc aatcctactt 4500 tagaacacc aaaaatgatg cgcatcaatg tattttatct tattttctca atctcctctc 4560 ctttcctcc acccataata agagaatgtt cctactcaca cttcagctgg gtcacatcca 4620 ccctccatt catccttcca tccatctttc catccattac ctccatccat ccttccaaca 4680 atatttatt gagtacctac tgtgtgccag gggctggtgg gacagtggtg acatagtctc 4740 gccctcata gagttgattg tctagtgagg aagacaagca tttttaaaaa ataaatttaa 4800 cttacaaac tttgtttgtc acaagtggtg tttattgcaa taaccgcttg gtttgcaacc 4860 ctttgctca acagaacata tgttgcaaga ccctcccatg ggggcacttg agttttggca 4920 ggctgacag agctctgggt tgtgcacatt tctttgcatt ccagctgtca ctctgtgcct 4980 tctacaact gattgcaaca gactgttgag ttatgataac accagtggga attgctggag 5040 aaccagagg cacttccacc ttggctggga agactatggt gctgccttgc ttctgtattt 5100 cttggattt tcctgaaagt gtttttaaat aaagaacaat tgttagaaaa aaaaaa 5156 131 671 DNA Homo sapien 131 aggtctggag ggcccacagc cggatgtggg acaccgggaa aaagtggtca tagcacacat 60 ttttgcatcc cggttgcagt gtgttgcaga cgaagtcctc ttgctcgtca ccccacactt 120 cctgggcagc caycacgagg atcatgactc ggaaaataaa gatgactgtg atccacacct 180 tcccgatgct ggtggagtgt ttgttgacac ccccgatgaa agtgtgcagc gtcccccaat 240 ccattgcgct ggtttatccc tgagtcctgt ttccaacgac tgccagtgtt tcagacccaa 300 agaatgaggg caagatccct ctgcgagggt ttcagacctc cttctcctac cccactggag 360 tgcctagaag ccaatgggtg cacagtgatg atacgaatgt caatctttgc tcggtcagtg 420 aggatgtcgc ctggaatatt caaattgaat tacagatgca tgaagagggc gtacaagtta 480 gaatttttct ttcgccatac agaaattgtt tagccagatc ttctgtactt cttttccttc 540 cctgaccctt cctgctcccc aggaagggag gtcagccccg tttgcaaaac acaggatgcc 600 cgtgacaccg gagacaggtc ttcttcaccg acaggaagtg ccttctggtg cctgcacgtt 660 ttaactgcta t 671 132 590 DNA Homo sapien 132 ctgaatggaa aagcttatgg ctctgtgatg atattagtga ccagcggaga tgataagctt 60 cttggcaatt gcttacccac tgtgctcagc agtggttcaa caattcactc cattgccctg 120 ggttcatctg cagccccaaa tctggaggaa ttatcacgtc ttacaggagg tttaaagttc 180 tttgttccag atatatcaaa ctccaatagc atgattgatg ctttcagtag aatttcctct 240 ggaactggag acattttcca gcaacatatt cagcttgaaa gtacaggtga aaatgtcaaa 300 cctcaccatc aattgaaaaa cacagtgact gtggataata ctgtgggcaa cgacactatg 360 tttctagtta cgtggcaggc cagtggtcct cctgagatta tattatttga tcctgatgga 420 cgaaaatact acacaaataa ttttatcacc aatctaactt ttcggacagc tagtctttgg 480 attccaggaa cagctaagcc tgggcactgg acttacaccc tgaacaatac ccatcattct 540 ctgcaagccc tgaaagtgac agtgacctct cgcgcctcca actcagacct 590 133 581 DNA Homo sapien 133 aggtcctgtc cgggggcact gagaactccc tctggaattc ttggggggtg ttggggagag 60 actgtgggcc tggagataaa acttgtctcc tctaccacca ccctgtaccc tagcctgcac 120 ctgtcctcat ctctgcaaag ttcagcttcc ttccccaggt ctctgtgcac tctgtcttgg 180 atgctctggg gagctcatgg gtggaggagt ctccaccaga gggaggctca ggggactggt 240 tgggccaggg atgaatattt gagggataaa aattgtgtaa gagccaaaga attggtagta 300 gggggagaac agagaggagc tgggctatgg gaaatgattt gaataatgga gctgggaata 360 tggctggata tctggtacta aaaaagggtc tttaagaacc tacttcctaa tctcttcccc 420 aatccaaacc atagctgtct gtccagtgct ctcttcctgc ctccagctct gccccaggct 480 cctcctagac tctgtccctg ggctagggca ggggaggagg gagagcaggg ttgggggaga 540 ggctgaggag agtgtgacat gtggggagag gaccagacct c 581 134 4797 DNA Homo sapien misc_feature (1)...(4797) n = A,T,C or G 134 cctgggacca aagtgctgcc cagagctgag ggtcctggag ccacatgaga aggcttctcc 60 ctgtgtacct gtgcagcaca gggtagggtg agtccactca gctgtctagg agaggaccca 120 ggagcagcag agacncgcca agcctttact cataccatat tctgatcctt ttccagcaaa 180 ttgtggctac taatttgccc cctgaagatc aagatggctc tggggatgac tctgacaact 240 tctccggctc aggtgcaggt gaggttgtca tgggggcccc ccccacccaa gacggcaaca 300 ggtcatgcct gggggcagtg gtcaggcagt ctcctgtgtt tactgagcat gtactgagtg 360 caccctgcct gccctgtctc cacccagctg gctccaaagg gcaatgctga ggagaggaat 420 ggggtcgtga gctgctgtta aggagagctc atgcttggag gtgaggtgaa ggctgtgagc 480 tccagaaggc cccagggcgc nctgctgcac gcaggctcat attcactagg aatagcttta 540 ctcactaaga aacctctgga acccccttca gaaggttatt tgactcctga gcctctattt 600 tctcatctgc aaaatgggaa taataccttg acctgataag cttgtggagc tgtaaggcag 660 cacagagcca gctggggtgt agctcttcca tccaagctcc cttccttact tcccctttcc 720 tgtggggact gggggagaga agtccctgag ctggaggtgg tcagggaagc ttcacagagg 780 aggtggctct tgagtggacc tcaggaagag gggtgagaga gctaaggaag gaggctgagg 840 tcatccctgg ggaagtgacc tagcggaggc ctgagagctg caaggtagga tatctgttgt 900 tggaagtgtc tgttgttgga agtgggggcc tttttttcag ggagggtggg gccagagaag 960 tgtgtgccct gggataagta ggataaccac agtagttatg cccctaaggg atgcccaccc 1020 cacccctgtg gtcacagaaa agctttccca ggtggcctag gcacctgtct cgtggctcca 1080 gagacaggct gcacctgaca cacacaatgg aaggacagct ctccttgtcc attttccaag 1140 gagcttagcc tcagctgcct tgtccaggta ctagcctccc tcatagcctg agcttggcca 1200 gcccaggtgc tctggagcct cccccgaccc acccaacaca ctctgcttct ggtcctcccc 1260 accccccacc tccccaacac actctgcttc tggtcctgca ggtgctttgc aagatatcac 1320 cttgtcacag cagaccccct ccacttggaa ggacacgcag ctcctgacgg ctattcccac 1380 gtctccagaa cccaccggcc tggaggctac agctgcctcc acctccaccc tgccggctgg 1440 agaggggccc aaggagggag aggctgtagt cctgccagaa gtggagcctg gcctcaccgc 1500 ccgggagcag gaggccaccc cccgacccag ggagaccaca cagctcccga ccactcatca 1560 ggcctcaacg accacagcca ccacggccca ggagcccgcc acctcccacc cccacaggga 1620 catgcagcct ggccaccatg agacctcaac ccctgcagga cccagccaag ctgaccttca 1680 cactccccac acagaggatg gaggtccttc tgccaccgag agggctgctg aggatggagc 1740 ctccagtcag ctcccagcag cagagggctc tggggagcag gtgagtggcc tctgcattcc 1800 ttgggaaatt gagtgggttg gtcctaatgc ctggcacttg gcaggcccta cacctgtgcc 1860 ctgcgcgatc tcgtattcct caccaggaag acagggcaca ggggccgcct tcccctaccc 1920 ccagggcctc gcagagcagg acagactaac tatgagatca gagcagaagc acccttaaag 1980 atcacccaag agagggctcc caaactcaca atccaaactt gcagccctcg tcgaagagtg 2040 aacgttatac cagtcatttt atttatagct tcgtggattt acgcttacac taaatagtct 2100 gctattcata caaaatgtgt gctttgtatc actttttgtg atatccatgc catggtccag 2160 ccagggtccg gagttgatgt ggcaagaagg cctggctttc gggccctgtg cgatcctggt 2220 ttgggtgcat ctgagtgggt ggtggcaaag atcagggagg caggagctgc ttctgggtct 2280 gtagtggagc tggttgctgc tgctggcggt gacctggcca acccaatctg cccctgccct 2340 cccacaggac ttcacctttg aaacctcggg ggagaatacg gctgtagtgg ccgtggagcc 2400 tgaccgccgg aaccagtccc cagtggatca gggggccacg ggggcctcac agggcctcct 2460 ggacaggaaa gaggtgctgg gaggtgagtt ttctttcagg ggggtagttt ggggtgaatt 2520 gctgctgtgg ggtcagggtg gggctgacca cagccaaggc cactgctttg ggagggtctg 2580 cacgagagcc caaggagccg ctgagctgag ctggccccgt ctacctgccc taggggtcat 2640 tgccggaggc ctcgtggggc tcatctttgc tgtgtgcctg gtgggtttca tgctgtaccg 2700 catgaagaag aaggacgaag gcagctactc cttggaggag ccgaaacaag ccaacggcgg 2760 ggcctaccag aagcccacca aacaggagga attctatgcc tgacgcggga gccatgcgcc 2820 ccctccgccc tgccactcac taggccccca cttgcctctt ccttgaagaa ctgcaggccc 2880 tggcctcccc tgccaccagg ccacctcccc agcattccag cccctctggt cgctcctgcc 2940 cacggagtcg tgggtgtgct gggagctcca ctctgcttct ctgacttctg cctggagact 3000 tagggcacca ggggtttctc gcataggacc tttccaccac agccagcacc tggcatcgca 3060 ccattctgac tcggtttctc caaactgaag cagcctctcc ccaggtccag ctctggaggg 3120 gagggggatc cgactgcttt ggacctaaat ggcctcatgt ggctggaaga tcctgcgggt 3180 ggggcttggg gctcacacac ctgtagcact tactggtagg accaagcatc ttgggggggt 3240 ggccgctgag tggcagggga caggagtcac tttgtttcgt ggggaggtct aatctagata 3300 tcgacttgtt tttgcacatg tttcctctag ttctttgttc atagcccagt agaccttgtt 3360 acttctgagg taagttaagt aagttgattc ggtatccccc catcttgctt ccctaatcta 3420 tggtcgggag acagcatcag ggttaagaag actttttttt ttttttttaa actaggagaa 3480 ccaaatctgg aagccaaaat gtaggcttag tttgtgtgtt gtctcttgag tttgtcgctc 3540 atgtgtgcaa cagggtatgg actatctgtc tggtggcccc gttctggtgg tctgttggca 3600 ggctggccag tccaggctgc cgtggggccg ccgcctcttt caagcagtcg tgcctgtgtc 3660 catgcgctca gggccatgct gaggcctggg ccgctgccac gttggagaag cccgtgtgag 3720 aagtgaatgc tgggactcag ccttcagaca gagaggactg tagggagggc ggcaggggcc 3780 tggagatcct cctgcaggct cacgcccgtc ctcctgtggc gccgtctcca ggggctgctt 3840 cctcctggaa attgacgagg ggtgtcttgg gcagagctgg ctctgagcgc ctccatccaa 3900 ggccaggttc tccgttagct cctgtggccc caccctgggc cctgggctgg aatcaggaat 3960 attttccaaa gagtgatagt cttttgcttt tggcaaaact ctacttaatc caatgggttt 4020 ttccctgtac agtagatttt ccaaatgtaa taaactttaa tataaagtag tctgtgaatg 4080 ccactgcctt cgcttcttgc ctctgtgctg tgtgtgacgt gaccggactt ttctgcaaac 4140 accaacatgt tgggaaactt ggctcgaatc tctgtgcctt cgtctttccc atggggaggg 4200 attctggttc cagggtccct ctgtgtattt gcttttttgt tttggctgaa attctcctgg 4260 aggtcggtag gttcagccaa ggttttataa ggctgatgtc aatttctgtg ttgccaagct 4320 ccaagcccat cttctaaatg gcaaaggaag gtggatggcc ccagcacagc ttgacctgag 4380 gctgtggtca cagcggaggt gtggagccga ggcctacccc ncagacacct tggacatcct 4440 cctcccaccc ggctgcagag gccaganncc agcccagggt cctgcactta cttgcttatt 4500 tgacaacgtt tcagcgactc cgttggccac tccgagagtg ggccagtctg tggatcagag 4560 atgcaccacc aagccaaggg aacctgtgtc cggtattcga tactgcgact ttctgcctgg 4620 agtgtatgac tgcacatgac tcgggggtgg ggaaaggggt cggctgacca tgctcatctg 4680 ctggtccgtg ggacggtncc caagccagag gtgggttcat ttgtgtaacg acaataaacg 4740 gtacttgtca tttcgggcaa cggctgctgt ggtggtggtt gagtctcttc ttggcct 4797 135 2856 DNA Homo sapien 135 tagtcgcggg tccccgagtg agcacgccag ggagcaggag accaaacgac gggggtcgga 60 gtcagagtcg cagtgggagt ccccggaccg gagcacgagc ctgagcggga gagcgccgct 120 cgcacgcccg tcgccacccg cgtacccggc gcagccagag ccaccagcgc agcgctgcca 180 tggagcccag cagcaagaag ctgacgggtc gcctcatgct ggctgtggga ggagcagtgc 240 ttggctccct gcagtttggc tacaacactg gagtcatcaa tgccccccag aaggtgatcg 300 aggagttcta caaccagaca tgggtccacc gctatgggga gagcatcctg cccaccacgc 360 tcaccacgct ctggtccctc tcagtggcca tcttttctgt tgggggcatg attggctcct 420 tctctgtggg ccttttcgtt aaccgctttg gccggcggaa ttcaatgctg atgatgaacc 480 tgctggcctt cgtgtccgcc gtgctcatgg gcttctcgaa actgggcaag tcctttgaga 540 tgctgatcct gggccgcttc atcatcggtg tgtactgcgg cctgaccaca ggcttcgtgc 600 ccatgtatgt gggtgaagtg tcacccacag cctttcgtgg ggccctgggc accctgcacc 660 agctgggcat cgtcgtcggc atcctcatcg cccaggtgtt cggcctggac tccatcatgg 720 gcaacaagga cctgtggccc ctgctgctga gcatcatctt catcccggcc ctgctgcagt 780 gcatcgtgct gcccttctgc cccgagagtc cccgcttcct gctcatcaac cgcaacgagg 840 agaaccgggc caagagtgtg ctaaagaagc tgcgcgggac agctgacgtg acccatgacc 900 tgcaggagat gaaggaagag agtcggcaga tgatgcggga gaagaaggtc accatcctgg 960 agctgttccg ctcccccgcc taccgccagc ccatcctcat cgctgtggtg ctgcagctgt 1020 cccagcagct gtctggcatc aacgctgtct tctattactc cacgagcatc ttcgagaagg 1080 cgggggtgca gcagcctgtg tatgccacca ttggctccgg tatcgtcaac acggccttca 1140 ctgtcgtgtc gctgtttgtg gtggagcgag caggccggcg gaccctgcac ctcataggcc 1200 tcgctggcat ggcgggttgt gccatactca tgaccatcgc gctagcactg ctggagcagc 1260 taccctggat gtcctatctg agcatcgtgg ccatctttgg ctttgtggcc ttctttgaag 1320 tgggtcctgg ccccatccca tggttcatcg tggctgaact cttcagccag ggtccacgtc 1380 cagctgccat tgccgttgca ggcttctcca actggacctc aaatttcatt gtgggcatgt 1440 gcttccagta tgtggagcaa ctgtgtggtc cctacgtctt catcatcttc actgtgctcc 1500 tggttctgtt cttcatcttc acctacttca aagttcctga gactaaaggc cggaccttcg 1560 atgagatcgc ttccggcttc cggcaggggg gagccagcca aagtgataag acacccgagg 1620 agctgttcca tcccctgggg gctgattccc aagtgtgagt cgccccagat caccagcccg 1680 gcctgctccc agcagcccta aggatctctc aggagcacag gcagctggat gagacttcca 1740 aacctgacag atgtcagccg agccgggcct ggggctcctt tctccagcca gcaatgatgt 1800 ccagaagaat attcaggact taacggctcc aggattttaa caaaagcaag actgttgctc 1860 aaatctattc agacaagcaa caggttttat aattttttta ttactgattt tgttattttt 1920 atatcagcct gagtctcctg tgcccacatc ccaggcttca ccctgaatgg ttccatgcct 1980 gagggtggag actaagccct gtcgagacac ttgccttctt cacccagcta atctgtaggg 2040 ctggacctat gtcctaagga cacactaatc gaactatgaa ctacaaagct tctatcccag 2100 gaggtggcta tggccacccg ttctgctggc ctggatctcc ccactctagg ggtcaggctc 2160 cattaggatt tgccccttcc catctcttcc tacccaacca ctcaaattaa tctttcttta 2220 cctgagacca gttgggagca ctggagtgca gggaggagag gggaagggcc agtctgggct 2280 gccgggttct agtctccttt gcactgaggg ccacactatt accatgagaa gagggcctgt 2340 gggagcctgc aaactcactg ctcaagaaga catggagact cctgccctgt tgtgtataga 2400 tgcaagatat ttatatatat ttttggttgt caatattaaa tacagacact aagttatagt 2460 atatctggac aagccaactt gtaaatacac cacctcactc ctgttactta cctaaacaga 2520 tataaatggc tggtttttag aaacatggtt ttgaaatgct tgtggattga gggtaggagg 2580 tttggatggg agtgagacag aagtaagtgg ggttgcaacc actgcaacgg cttagacttc 2640 gactcaggat ccagtccctt acacgtacct ctcatcagtg tcctcttgct caaaaatctg 2700 tttgatccct gttacccaga gaatatatac attctttatc ttgacattca aggcatttct 2760 atcacatatt tgatagttgg tgttcaaaaa aacactagtt ttgtgccagc cgtgatgctc 2820 aggcttgaaa tcgcattatt ttgaatgtga agggaa 2856 136 356 DNA Homo sapien 136 ggtggagcca aatgaagaaa atgaagatga aagagacaga cacctcagtt tttctggatc 60 aggcattgat gatgatgaag attttatctc cagcaccatt tcaaccacac cacgggcttt 120 tgaccacaca aaacagaacc aggactggac tcagtggaac ccaagccatt caaatccgga 180 agtgctactt cagacaacca caaggatgac tgatgtagac agaaatggca ccactgctta 240 tgaaggaaac tggaacccag aagcacaccc tcccctcatt caccatgagc atcatgagga 300 agaagagacc ccacattcta caagcacaat ccaggcaact cctagtagta caacgg 356 137 356 DNA Homo sapien misc_feature (1)...(356) n = A,T,C or G 137 gcaggtggag aagacatttt attgttcctg gggtctctgg aggcccattg gtggggctgg 60 gtcactggct gcccccggaa cagggcgctg ctccatggct ctgcttgtgg tagtctgtgg 120 ctatgtctcc cagcaaggac agaaactcag aaaaatcaat cttcttatcc tcattcttgt 180 cctttttctc aaagacatcg gcgaggtaat ttgtgccctt tttacctcgg cccgcgacca 240 cgctaaggcc aaanttccag acanayggcc gggccggtnc nataggggan cccaacttgg 300 ggacccaaac tctggcgcgg aaacacangg gcataagctt gnttcctgtg gggaaa 356 138 353 DNA Homo sapien 138 aggtccagtc ctccacttgg cctgatgaga gtggggagtg gcaagggacg tttctcctgc 60 aatagacact tagatttctc tcttgtggga agaaaccacc tgtccatcca ctgactcttc 120 tacattgatg tggaaattgc tgctgctacc accacctcct gaagaggctt ccctgatgcc 180 aatgccagcc atcttggcat cctggccctc gagcaggctg cggtaagtag cgatctcctg 240 ctccagccgt gtctttatgt caagcagcat cttgtactcc tggttctgag cctccatctc 300 gcatcggagc tcactcagac ctcgsccgsg mssmcgctam gccgaattcc agc 353 139 371 DNA Homo sapien 139 agcgtggtcg cggccgaggt ccatccgaag caagattgca gatggcagtg tgaagagaga 60 agacatattc tacacttcaa agctttggtg caattcccat cgaccagagt tggtccgacc 120 agccttggaa aggtcactga aaaatcttca attggattat gttgacctct accttattca 180 ttttccagtg tctgtaaagc caggtgagga agtgatccca aaagatgaaa atggaaaaat 240 actatttgac acagtggatc tctgtgccac gtgggaggcc gtggagaagt gtaaagatgc 300 aggattggac ctgcccgggc ggccgctcga aagccgaatt ccagcacact ggcggccgtt 360 actagtggat c 371 140 370 DNA Homo sapien 140 tagcgtggtc gcggccgagg tccatctccc tttgggaact agggggctgc tggtgggaaa 60 tgggagccag ggcagatgtt gcattccttt gtgtccctgt aaatgtggga ctacaagaag 120 aggagctgcc tgagtggtac tttctcttcc tggtaatcct ctggcccagc ctcatggcag 180 aatagaggta tttttaggct atttttgtaa tatggcttct ggtcaaaatc cctgtgtagc 240 tgaattccca agccctgcat tgtacagccc cccactcccc tcaccaccta ataaaggaat 300 agttaacact caaaaaaaaa aaaaaacctg cccgggcggc cgctcgaaag ccgaattcca 360 gcacactggc 370 141 371 DNA Homo sapien 141 tagcgtggtc gcggccgagg tcctctgtgc tgcctgtcac agcccgatgg taccagcgca 60 gggtgtaggc agtgcaggag ccctcatcca gtggcaggga acaggggtca tcactatccc 120 aaggagcttc agggtcctgg tactcctcca cagaatactc ggagtattca gagtactcat 180 catcctcagg gggtacccgc tcttcctcct ctgcatgaga gacgcggagc acaggcacag 240 catggagctg ggagccggca gtgtctgcag cataactagg gaggggtcgt gatccagatg 300 cgatgaactg gccctggcag gcacagtgct gactcatctc ttggcgacct gcccgggcgg 360 ccgctcgaag c 371 142 343 DNA Homo sapien 142 gcgttttgag gccaatggtg taaaaggaaa tatcttcaca taaaaactag atggaagcat 60 tgtcagaaac ctctttgtga tgtttgcttt caactcacag agttgaacat tccttttcat 120 agagcagttt tgaaacactc ttttgtagaa tttgcaagcg gatgattgga tcgctatgag 180 gtcttcattg gaaacgggat acctttacat aaaaactaga cagtagcatt ctcagaaatt 240 tctttgggat gtgggcattc aacccacaga ggagaacttc atttgataga gcagttttga 300 aacacccttt ttgtagaatc tacaggtgga catttagagt gct 343 143 354 DNA Homo sapien 143 aggtctgatg gcagaaaaac tcagactgtc tgcaacttta cagatggtgc attggttcag 60 catcaggagt gggatgggaa ggaaagcaca ataacaagaa aattgaaaga tgggaaatta 120 gtggtggagt gtgtcatgaa caatgtcacc tgtactcgga tctatgaaaa agtagaataa 180 aaattccatc atcactttgg acaggagtta attaagagaa tgaccaagct cagttcaatg 240 agcaaatctc catactgttt ctttcttttt tttttcatta ctgtgttcaa ttatctttat 300 cataaacatt ttacatgcag ctatttcaaa gtgtgttgga ttaattagga tcat 354 144 353 DNA Homo sapien 144 ggtcaaggac ctgggggacc cccaggtcca gcagccacat gattctgcag cagacaggga 60 cctagagcac atctggatct cagccccacc cctggcaacc tgcctgccta gagaactccc 120 aagatgacag actaagtagg attctgccat ttagaataat tctggtatcc tgggcgttgc 180 gttaagttgc ttaactttca ttctgtctta cgatagtctt cagaggtggg aacagatgaa 240 gaaaccatgc cccagagaag gttaagtgac ttcctcttta tggagccagt gttccaacct 300 aggtttgcct gataccagac ctgtggcccc acctcccatg caggtctctg tgg 353 145 371 DNA Homo sapien 145 caggtctgtc ataaactggt ctggagtttc tgacgactcc ttgttcacca aatgcaccat 60 ttcctgagac ttgctggcct ctccgttgag tccacttggc tttctgtcct ccacagctcc 120 attgccactg ttgatcacta gctttttctt ctgcccacac cttcttcgac tgttgactgc 180 aatgcaaact gcaagaatca aagccaaggc caagagggat gccaagatga tcagccattc 240 tggaatttgg ggtgtcctta taggaccaga ggttgtgttt gctccacctt cttgactccc 300 atgtgagacc tcggccgcga ccacgctaag ccgaattcca gcacactggc ggcccgttac 360 tagtggatcc g 371 146 355 DNA Homo sapien 146 ggtcctccgt cctcttccca gaggtgtcgg ggcttggccc cagcctccat cttcgtctct 60 caggatggcg agtagcagcg gctccaaggc tgaattcatt gtcggaggga aatataaact 120 ggtacggaag atcgggtctg gctccttcgg ggacatctat ttggcgatca acatcaccaa 180 cggcgaggaa gtggcagtga agctagaatc tcagaaggcc aggcatcccc agttgctgta 240 cgagagcaag ctctataaga ttcttcaagg tggggttggc atcccccaca tacggtggta 300 tggtcaggaa aaagactaca atgtactagt catggatctt ctgggaccta gcctc 355 147 355 DNA Homo sapien 147 ggtctgttac aaaatgaaga cagacaacac aacatttact ctgtggagat atcctactca 60 tactatgcac gtgctgtgat tttgaacata actcgtccca aaaacttgtc acgatcatcc 120 tgacttttta ggttggctga tccatcaatc ttgcactcaa ctgttacttc tttcccagtg 180 ttgttaggag caaagctgac ctgaacagca accaatggct gtagataccc aacatgcagt 240 tttttcccat aatatgggaa atattttaag tctatcattc cattatgagg ataaactgct 300 acatttggta tatcttcatt ctttgaaaca caatctatcc ttggcactcc ttcag 355 148 369 DNA Homo sapien 148 aggtctctct ccccctctcc ctctcctgcc agccaagtga agacatgctt acttcccctt 60 caccttcctt catgatgtgg gaagagtgct gcaacccagc cctagccaac accgcatgag 120 agggagtgtg ccgagggctt ctgagaaggt ttctctcaca tctagaaaga agcgcttaag 180 atgtggcagc ccctcttctt caagtggctc ttgtcctgtt gccctgggag ttctcaaatt 240 gctgcagcag cctccatcca gcctgaggat gacatcaata cacagaggaa gaagagtcag 300 gaaaagatga gagaagttac agactctcct gggcgacccc gagagcttac cattcctcag 360 acttcttca 369 149 620 DNA Homo sapien misc_feature (1)...(620) n = A,T,C or G 149 actagtcaaa aatgctaaaa taatttggga gaaaatattt tttaagtagt gttatagttt 60 catgtttatc ttttattatg ttttgtgaag ttgtgtcttt tcactaatta cctatactat 120 gccaatattt ccttatatct atccataaca tttatactac atttgtaana naatatgcac 180 gtgaaactta acactttata aggtaaaaat gaggtttcca anatttaata atctgatcaa 240 gttcttgtta tttccaaata gaatggactt ggtctgttaa gggctaagga gaagaggaag 300 ataaggttaa aagttgttaa tgaccaaaca ttctaaaaga aatgcaaaaa aaaagtttat 360 tttcaagcct tcgaactatt taaggaaagc aaaatcattt cctaaatgca tatcatttgt 420 gagaatttct cattaatatc ctgaatcatt catttcacta aggctcatgt tnactccgat 480 atgtctctaa gaaagtacta tttcatggtc caaacctggt tgccatantt gggtaaaggc 540 tttcccttaa gtgtgaaant atttaaaatg aaattttcct ctttttaaaa attctttana 600 agggttaagg gtgttgggga 620 150 371 DNA Homo sapien 150 ggtccgatca aaacctgcta cctccccaag actttactag tgccgataaa ctttctcaaa 60 gagcaaccag tatcacttcc ctgtttataa aacctctaac catctctttg ttctttgaac 120 atgctgaaaa ccacctggtc tgcatgtatg cccgaatttg yaattctttt ctctcaaatg 180 aaaatttaat tttagggatt catttctata ttttcacata tgtagtatta ttatttcctt 240 atatgtgtaa ggtgaaattt atggtatttg agtgtgcaag aaaatatatt tttaaagctt 300 tcatttttcc cccagtgaat gatttagaat tttttatgta aatatacaga atgttttttc 360 ttacttttat a 371 151 4655 DNA Homo sapien 151 gggacttgag ttctgttatc ttcttaagta gattcatatt gtaagggtct cggggtgggg 60 gggttggcaa aatcctggag ccagaagaaa ggacagcagc attgatcaat cttacagcta 120 acatgttgta cctggaaaac aatgcccaga ctcaatttag tgagccacag tacacgaacc 180 tggggctcct gaacagcatg gaccagcaga ttcagaacgg ctcctcgtcc accagtccct 240 ataacacaga ccacgcgcag aacagcgtca cggcgccctc gccctacgca cagcccagct 300 ccaccttcga tgctctctct ccatcacccg ccatcccctc caacaccgac tacccaggcc 360 cgcacagttt cgacgtgtcc ttccagcagt cgagcaccgc caagtcggcc acctggacgt 420 attccactga actgaagaaa ctctactgcc aaattgcaaa gacatgcccc atccagatca 480 aggtgatgac cccacctcct cagggagctg ttatccgcgc catgcctgtc tacaaaaaag 540 ctgagcacgt cacggaggtg gtgaagcggt gccccaacca tgagctgagc cgtgaattca 600 acgagggaca gattgcccct yctagtcatt tgattcgagt agaggggaac agccatgccc 660 agtatgtaga agatcccatc acaggaagac agagtgtgct ggtaccttat gagccacccc 720 aggttggcac tgaattcacg acagtcttgt acaatttcat gtgtaacagc agttgtgttg 780 gagggatgaa ccgccgtcca attttaatca ttgttactct ggaaaccaga gatgggcaag 840 tcctgggccg acgctgcttt gaggcccgga tctgtgcttg cccaggaaga gacaggaagg 900 cggatgaaga tagcatcaga aagcagcaag tttcggacag tacaaagaac ggtgatggta 960 cgaagcgccc gtttcgtcag aacacacatg gtatccagat gacatccatc aagaaacgaa 1020 gatccccaga tgatgaactg gtatacttac cagtgagggg ccgtgagact tatgaaatgc 1080 tggtgaagat caaagagtcc ctggaactca tgcagtacct tcttcagcac acaattgaaa 1140 cgtacaggca acagcaacag cagcagcacc agcacttact tcagaaacag acctcaatac 1200 agtctccatc ttcatatggt aacagctccc cacctctgaa caaaatgaac agcatgaaca 1260 agctgccttc tgtgagccag cttatcaacc ctcagcagcg caacgccctc actcctacaa 1320 ccattcctga tggcatggga gccaacattc ccatgatggg cacccacatg ccaatggctg 1380 gagacatgaa tggactcagc cccacccagg cactccctcc cccactctcc atgccatcca 1440 cctcccactg cacaccccca cctccgtatc ccacagattg cagcattgtc agtttcttag 1500 cgaggttggg ctgttcatca tgtctggact atttcacgac ccaggggctg accaccatct 1560 atcagattga gcattactcc atggatgatc tggcaagtct gaaaatccct gagcaatttc 1620 gacatgcgat ctggaagggc atcctggacc accggcagct ccacgaattc tcctcccctt 1680 ctcatctcct gcggacccca agcagtgcct ctacagtcag tgtgggctcc agtgagaccc 1740 ggggtgagcg tgttattgat gctgtgcgat tcaccctccg ccagaccatc tctttcccac 1800 cccgagatga gtggaatgac ttcaactttg acatggatgc tcgccgcaat aagcaacagc 1860 gcatcaaaga ggagggggag tgagcctcac catgtgagct cttcctatcc ctctcctaac 1920 tgccagcccc ctaaaagcac tcctgcttaa tcttcaaagc cttctcccta gctcctcccc 1980 ttcctcttgt ctgatttctt aggggaagga gaagtaagag gcttacttct taccctaacc 2040 atctgacctg gcatctaatt ctgattctgg ctttaagcct tcaaaactat agcttgcaga 2100 actgtagctt gccatggcta ggtagaagtg agcaaaaaag agttgggtgt ctccttaagc 2160 tgcagagatt tctcattgac ttttataaag catgttcacc cttatagtct aagactatat 2220 atataaatgt ataaatatac agtatagatt tttgggtggg gggcattgag tattgtttaa 2280 aatgtaattt aaatgaaaga aaattgagtt gcacttattg accatttttt aatttacttg 2340 ttttggatgg cttgtctata ctccttccct taaggggtat catgtatggt gataggtatc 2400 tagagcttaa tgctacatgt gagtgacgat gatgtacaga ttctttcagt tctttggatt 2460 ctaaatacat gccacatcaa acctttgagt agatccattt ccattgctta ttatgtaggt 2520 aagactgtag atatgtattc ttttctcagt gttggtatat tttatattac tgacatttct 2580 tctagtgatg atggttcacg ttggggtgat ttaatccagt tataagaaga agttcatgtc 2640 caaacgtcct ctttagtttt tggttgggaa tgaggaaaat tcttaaaagg cccatagcag 2700 ccagttcaaa aacacccgac gtcatgtatt tgagcatatc agtaaccccc ttaaatttaa 2760 taccagatac cttatcttac aatattgatt gggaaaacat ttgctgccat tacagaggta 2820 ttaaaactaa atttcactac tagattgact aactcaaata cacatttgct actgttgtaa 2880 gaattctgat tgatttgatt gggatgaatg ccatctatct agttctaaca gtgaagtttt 2940 actgtctatt aatattcagg gtaaatagga atcattcaga aatgttgagt ctgtactaaa 3000 cagtaagata tctcaatgaa ccataaattc aactttgtaa aaatcttttg aagcatagat 3060 aatattgttt ggtaaatgtt tcttttgttt ggtaaatgtt tcytttaaag accctcctat 3120 tctataaaac tctgcatgta gaggcttgtt tacctttctc tctctaaggt ttacaatagg 3180 agtggtgatt tgaaaaatat aaaattatga gattggtttt cctgtggcat aaattgcatc 3240 actgtatcat tttctttttt aaccggtaag agtttcagtt tgttggaaag taactgtgag 3300 aacccagttt cccgtccatc tcccttaggg actacccata gacatgaaag gtccccacag 3360 agcaagagat aagtctttca tggctgctgt tgcttaaacc acttaaacga agagttccct 3420 tgaaactttg ggaaaacatg ttaatgacaa tattccagat ctttcagaaa tataacacat 3480 ttttttgcat gcatgcaaat gagctctgaa atcttcccat gcattctggt caagggctgt 3540 cattgcacat aagcttccat tttaatttta aagtgcaaaa gggccagcgt ggctctaaaa 3600 ggtaatgtgt ggattgcctc tgaaaagtgt gtatatattt tgtgtgaaat tgcatacttt 3660 gtattttgat tatttttttt ttcttcttgg gatagtggga tttccagaac cacacttgaa 3720 accttttttt atcgtttttg tattttcatg aaaataccat ttagtaagaa taccacatca 3780 aataagaaat aatgctacaa ttttaagagg ggagggaagg gaaagttttt ttttttatta 3840 tttttttaaa attttgtatg ttaaagagaa tgagtccttg atttcaaagt tttgttgtac 3900 ttaaatggta ataagcactg taaacttctg caacaagcat gcagctttgc aaacccatta 3960 aggggaagaa tgaaagctgt tccttggtcc tagtaagaag acaaactgct tcccttactt 4020 tgctgagggt ttgaataaac ctaggacttc cgagctatgt cagtactatt caggtaacac 4080 tagggccttg gaaatccctg tactgtgtct catggatttg gcactagcca aagcgaggca 4140 ccccttactg gcttacctcc tcatggcagc ctactctcct tgagtgtatg agtagccagg 4200 gtaaggggta aaaggatagt aagcatagaa accactagaa agtgggctta atggagttct 4260 tgtggcctca gctcaatgca gttagctgaa gaattgaaaa gtttttgttt ggagacgttt 4320 ataaacagaa atggaaagca gagttttcat taaatccttt tacctttttt ttttcttggt 4380 aatcccctaa aataacagta tgtgggatat tgaatgttaa agggatattt ttttctatta 4440 tttttataat tgtacaaaat taagcaaatg ttaaaagttt tatatgcttt attaatgttt 4500 tcaaaaggta ttatacatgt gatacatttt ttaagcttca gttgcttgtc ttctggtact 4560 ttctgttatg ggcttttggg gagccagaag ccaatctaca atctcttttt gtttgccagg 4620 acatgcaata aaatttaaaa aataaataaa aacta 4655 152 586 PRT Homo sapien 152 Met Leu Tyr Leu Glu Asn Asn Ala Gln Thr Gln Phe Ser Glu Pro Gln 1 5 10 15 Tyr Thr Asn Leu Gly Leu Leu Asn Ser Met Asp Gln Gln Ile Gln Asn 20 25 30 Gly Ser Ser Ser Thr Ser Pro Tyr Asn Thr Asp His Ala Gln Asn Ser 35 40 45 Val Thr Ala Pro Ser Pro Tyr Ala Gln Pro Ser Ser Thr Phe Asp Ala 50 55 60 Leu Ser Pro Ser Pro Ala Ile Pro Ser Asn Thr Asp Tyr Pro Gly Pro 65 70 75 80 His Ser Phe Asp Val Ser Phe Gln Gln Ser Ser Thr Ala Lys Ser Ala 85 90 95 Thr Trp Thr Tyr Ser Thr Glu Leu Lys Lys Leu Tyr Cys Gln Ile Ala 100 105 110 Lys Thr Cys Pro Ile Gln Ile Lys Val Met Thr Pro Pro Pro Gln Gly 115 120 125 Ala Val Ile Arg Ala Met Pro Val Tyr Lys Lys Ala Glu His Val Thr 130 135 140 Glu Val Val Lys Arg Cys Pro Asn His Glu Leu Ser Arg Glu Phe Asn 145 150 155 160 Glu Gly Gln Ile Ala Pro Ser Ser His Leu Ile Arg Val Glu Gly Asn 165 170 175 Ser His Ala Gln Tyr Val Glu Asp Pro Ile Thr Gly Arg Gln Ser Val 180 185 190 Leu Val Pro Tyr Glu Pro Pro Gln Val Gly Thr Glu Phe Thr Thr Val 195 200 205 Leu Tyr Asn Phe Met Cys Asn Ser Ser Cys Val Gly Gly Met Asn Arg 210 215 220 Arg Pro Ile Leu Ile Ile Val Thr Leu Glu Thr Arg Asp Gly Gln Val 225 230 235 240 Leu Gly Arg Arg Cys Phe Glu Ala Arg Ile Cys Ala Cys Pro Gly Arg 245 250 255 Asp Arg Lys Ala Asp Glu Asp Ser Ile Arg Lys Gln Gln Val Ser Asp 260 265 270 Ser Thr Lys Asn Gly Asp Gly Thr Lys Arg Pro Phe Arg Gln Asn Thr 275 280 285 His Gly Ile Gln Met Thr Ser Ile Lys Lys Arg Arg Ser Pro Asp Asp 290 295 300 Glu Leu Val Tyr Leu Pro Val Arg Gly Arg Glu Thr Tyr Glu Met Leu 305 310 315 320 Val Lys Ile Lys Glu Ser Leu Glu Leu Met Gln Tyr Leu Leu Gln His 325 330 335 Thr Ile Glu Thr Tyr Arg Gln Gln Gln Gln Gln Gln His Gln His Leu 340 345 350 Leu Gln Lys Gln Thr Ser Ile Gln Ser Pro Ser Ser Tyr Gly Asn Ser 355 360 365 Ser Pro Pro Leu Asn Lys Met Asn Ser Met Asn Lys Leu Pro Ser Val 370 375 380 Ser Gln Leu Ile Asn Pro Gln Gln Arg Asn Ala Leu Thr Pro Thr Thr 385 390 395 400 Ile Pro Asp Gly Met Gly Ala Asn Ile Pro Met Met Gly Thr His Met 405 410 415 Pro Met Ala Gly Asp Met Asn Gly Leu Ser Pro Thr Gln Ala Leu Pro 420 425 430 Pro Pro Leu Ser Met Pro Ser Thr Ser His Cys Thr Pro Pro Pro Pro 435 440 445 Tyr Pro Thr Asp Cys Ser Ile Val Ser Phe Leu Ala Arg Leu Gly Cys 450 455 460 Ser Ser Cys Leu Asp Tyr Phe Thr Thr Gln Gly Leu Thr Thr Ile Tyr 465 470 475 480 Gln Ile Glu His Tyr Ser Met Asp Asp Leu Ala Ser Leu Lys Ile Pro 485 490 495 Glu Gln Phe Arg His Ala Ile Trp Lys Gly Ile Leu Asp His Arg Gln 500 505 510 Leu His Glu Phe Ser Ser Pro Ser His Leu Leu Arg Thr Pro Ser Ser 515 520 525 Ala Ser Thr Val Ser Val Gly Ser Ser Glu Thr Arg Gly Glu Arg Val 530 535 540 Ile Asp Ala Val Arg Phe Thr Leu Arg Gln Thr Ile Ser Phe Pro Pro 545 550 555 560 Arg Asp Glu Trp Asn Asp Phe Asn Phe Asp Met Asp Ala Arg Arg Asn 565 570 575 Lys Gln Gln Arg Ile Lys Glu Glu Gly Glu 580 585 153 2007 DNA Homo sapien 153 gaattcgtcg ctgctccagg gaaagttctg ttactccact gactctctct tttcctgata 60 acatggccag caagaaagta attacagtgt ttggagcaac aggagctcaa ggtggctctg 120 tggccagggc aattttggag agcaaaaaat ttgcagtgag agcagtgacc agggatgtga 180 cttgaccaaa tgccctggag ctccagcgcc ttggagctga ggtggtcaaa ggtgacctga 240 atgataaagc atcggtggac agtgccttaa aaggtgtcta tggggccttc ttggtgacca 300 acttctggga ccctctcaac caagataagg aagtgtgtcg ggggaagctg gtggcagact 360 ccgccaagca cctgggtctg aagcacgtgg tgtacagcgg cctggagaac gtcaagcgac 420 tgacggatgg caagctggag gtgccgcact ttgacagcaa gggcgaggtg gaggagtact 480 tctggtccat tggcatcccc atgaccagtg tccgcgtggc ggcctacttt gaaaactttc 540 tcgcggcgtg gcggcccgtg aaagcctctg atggagatta ctacaccttg gctgtaccga 600 tgggagatgt accaatggat ggtatctctg ttgctgatat tggagcagcc gtctctagca 660 tttttaattc tccagaggaa tttttaggca aggccgtggg gctcagtgca gaagcactaa 720 caatacagca atatgctgat gttttgtcca aggctttggg gaaagaagtc cgagatgcaa 780 agattacccc ggaagctttc gagaagctgg gattccctgc agcaaaggaa atagccaata 840 tgtgtcgttt ctatgaaatg aagccagacc gagatgtcaa tctcacccac caactaaatc 900 ccaaagtcaa aagcttcagc cagtttatct cagagaacca gggagccttc aagggcatgt 960 agaaaatcag ctgttcagat aggcctctgc accacacagc ctctttcctc tctgatcctt 1020 ttcctcttta cggcacaaca ttcatgttga cagaacatgc tggaatgcaa ttgtttgcaa 1080 caccgaagga tttcctgcgg tcgcctcttc agtaggaagc actgcattgg tgataggaca 1140 cggtaatttg attcacattt aacttgctag ttagtgataa gggtggtaca actgtttggt 1200 aaaatgagaa gcctcggaac ttggagcttc tctcctacca ctaatgggag ggcagattat 1260 actgggattt ctcctgggtg agtaatttca agccctaatg ctgaaattcc cctaggcagc 1320 tccagttttc tcaactgcat tgcaaaattc ccagtgaact tttaagtact tttaacttaa 1380 aaaaatgaac atctttgtag agaattttct ggggaacatg gtgttcaatg aacaagcaca 1440 agcattggaa atgctaaaat tcagttttgc ctcaagattg gaagtttatt ttctgactca 1500 ttcatgaagt catctattga gccaccattc aattattcat ctattaattc cttgatcctt 1560 catttatcca ttctgcaaac ttttcttgag caccagcacg ggtggccatt tgtggacttc 1620 tcttcattcc tatgtgtttt cttatcaaag tgatccactc tcgaaaggct cctttccagt 1680 ctgtggttgg gttcaagtca tgccagggcc agggggccca tctcctcgtt tagctctagg 1740 caaaatccag gggatctgca gtggggagcg ggggcaggaa gctggaggga aggcctgtga 1800 agggtaggga tgtggaaaga caaggtgaca gaaggaccca ataggacctt tctatatctc 1860 tggcttagca ttttctacat catattgtaa tcgtcttatt tgctagtttt cttccttact 1920 gtgagtgact aacagtcatc tttatcccag tgcctggtac ataataagtg atcaataaat 1980 gttgattgac taaaaaaaaa aaaaaaa 2007 154 2148 DNA Homo sapien 154 gaattcgtcg ctgctccagg gaaagttctg ttactccact gactctctct tttcctgata 60 acatggccag caagaaagta attacagtgt ttggagcaac aggagctcaa ggtggctctg 120 tggccagggc aattttggag agcaaaaaat ttgcagtgag agcagtgacc agggatgtga 180 cttgaccaaa tgccctggag ctccagcgcc ttggagctga ggtggtcaaa ggtgacctga 240 atgataaagc atcggtggac agtgccttaa aaggggaagc tggtggcaga ctccgccaag 300 cacctgggtc tgaagcacgt ggtgtacagc ggcctggaga acgtcaagcg actgacggat 360 ggcaagctgg aggtgccgca ctttgacagc aagggcgagg tggaggagta cttctggtcc 420 attggcatcc ccatgaccag tgtccgcgtg gcggcctact ttgaaaactt tctcgcggcg 480 tggcggcccg tgaaagcctc tgatggagat tactacacct tggctgtacc gatgggagat 540 gtaccaatgg atggtatctc tgttgctgat attggagcag ccgtctctag catttttaat 600 tctccagagg aatttttagg caaggccgtg gggctcagtg cagaagcact aacaatacag 660 caatatgctg atgttttgtc caaggctttg gggaaagaag tccgagatgc aaagactatc 720 tgtgctatag atgaccagaa aacagtggaa gaaggtttca tggaagacgt gggcttgagt 780 tggtccttga gggaacatga ccatgtatag acagaggagg catcaagaag gctggcctgg 840 ctaattctgg aataaacacg acaaaccaga ggcagtacgg gaaggaggca aattctggct 900 ctgcctctat ccttgattac cccggaagct ttcgagaagc tgggattccc tgcagcaaag 960 gaaatagcca atatgtgtcg tttctatgaa atgaagccag accgagatgt caatctcacc 1020 caccaactaa atcccaaagt caaaagcttc agccatttta tctcagagaa ccagggagcc 1080 ttcaagggca tgtagaaaat cagctgttca gataggcctc tgcaccacac agcctctttc 1140 ctctctgatc cttttcctct ttacggcaca acattcatgt tgacagaaca tgctggaatg 1200 caattgtttg caacaccgaa ggatttcctg cggtcgcctc ttcagtagga agcactgcat 1260 tggtgatagg acacggtaat ttgattcaca tttaacttgc tagttagtga taagggtggt 1320 acaactgttt ggtaaaatga gaagcctcgg aacttggagc ttctctccta ccactaatgg 1380 gagggcagat tatactggga tttctcctgg gtgagtaatt tcaagcccta atgctgaaat 1440 tcccctaggc agctccagtt ttctcaactg cattgcaaaa ttcccagtga acttttaagt 1500 acttttaact taaaaaaatg aacatctttg tagagaattt tctggggaac atggtgttca 1560 atgaacaagc acaagcattg gaaatgctaa aattcagttt tgcctcaaga ttggaagttt 1620 attttctgac tcattcatga agtcatctat tgagccacca ttcaattatt catctattaa 1680 ttccttgatc cttcatttat ccattctgca aacttttctt gagcaccagc acgggtggcc 1740 atttgtggac ttctcttcat tcctatgtgt tttcttatca aagtgatcca ctctcgaaag 1800 gctcctttcc agtctgtggt tgggttcaag tcatgccagg gccagggggc ccatctcctc 1860 gtttagctct aggcaaaatc caggggatct gcagtgggga gcgggggcag gaagctggag 1920 ggaaggcctg tgaagggtag ggatgtggaa agacaaggtg acagaaggac ccaataggac 1980 ctttctatat ctctggctta gcattttcta catcatattg taatcgtctt atttgctagt 2040 tttcttcctt actgtgagtg actaacagtc atctttatcc cagtgcctgg tacataataa 2100 gtgatcaata aatgttgatt gactaaatga aaaaaaaaaa aaaaaaaa 2148 155 153 PRT Homo sapien 155 Met Thr Ser Val Arg Val Ala Ala Tyr Phe Glu Asn Phe Leu Ala Ala 1 5 10 15 Trp Arg Pro Val Lys Ala Ser Asp Gly Asp Tyr Tyr Thr Leu Ala Val 20 25 30 Pro Met Gly Asp Val Pro Met Asp Gly Ile Ser Val Ala Asp Ile Gly 35 40 45 Ala Ala Val Ser Ser Ile Phe Asn Ser Pro Glu Glu Phe Leu Gly Lys 50 55 60 Ala Val Gly Leu Ser Ala Glu Ala Leu Thr Ile Gln Gln Tyr Ala Asp 65 70 75 80 Val Leu Ser Lys Ala Leu Gly Lys Glu Val Arg Asp Ala Lys Ile Thr 85 90 95 Pro Glu Ala Phe Glu Lys Leu Gly Phe Pro Ala Ala Lys Glu Ile Ala 100 105 110 Asn Met Cys Arg Phe Tyr Glu Met Lys Pro Asp Arg Asp Val Asn Leu 115 120 125 Thr His Gln Leu Asn Pro Lys Val Lys Ser Phe Ser Gln Phe Ile Ser 130 135 140 Glu Asn Gln Gly Ala Phe Lys Gly Met 145 150 156 128 PRT Homo sapien 156 Met Thr Ser Val Arg Val Ala Ala Tyr Phe Glu Asn Phe Leu Ala Ala 1 5 10 15 Trp Arg Pro Val Lys Ala Ser Asp Gly Asp Tyr Tyr Thr Leu Ala Val 20 25 30 Pro Met Gly Asp Val Pro Met Asp Gly Ile Ser Val Ala Asp Ile Gly 35 40 45 Ala Ala Val Ser Ser Ile Phe Asn Ser Pro Glu Glu Phe Leu Gly Lys 50 55 60 Ala Val Gly Leu Ser Ala Glu Ala Leu Thr Ile Gln Gln Tyr Ala Asp 65 70 75 80 Val Leu Ser Lys Ala Leu Gly Lys Glu Val Arg Asp Ala Lys Thr Ile 85 90 95 Cys Ala Ile Asp Asp Gln Lys Thr Val Glu Glu Gly Phe Met Glu Asp 100 105 110 Val Gly Leu Ser Trp Ser Leu Arg Glu His Asp His Val Ala Gly Ala 115 120 125 157 424 DNA Homo sapien misc_feature (1)...(424) n = A,T,C or G 157 ctgcagcccg ggggatccac tagtccagtg tggtggaatt cattggtctt tacaagactt 60 ggatacatta cagcagacat ggaaatataa ttttaaaaaa tttctctcca acctccttca 120 aattcagtca ccactgttat attaccttct ccaggaaccc tccagtgggg aaggctgcga 180 tattagattt ccttgtatgc aaagtttttg ttgaaagctg tgctcagagg aggtgagagg 240 agaggaagga gaaaactgca tcataacttt acagaattga atctagagtc ttccccgaaa 300 agcccagaaa cttctctgcn gnatctggct tgtccatctg gtctaaggtg gctgcttctt 360 ccccagccat cgagtcagtt tgtgcccatg aataatacac gacctgctat ttcccatgac 420 tgct 424 158 2099 DNA Homo sapien 158 ccgcggttaa aaggcgcagc aggtgggagc cggggccttc acccgaaacc cgacgagagc 60 ccgacagccg gcggcgcccg agcccgacct gcctgcccag ccggagcgaa gggcgccgcc 120 ccgcgcagag cccgcgccag ggccgccggc cgcagagcag ttaaaacgtg caggcaccag 180 aaggcacttc ctgtcggtga agaagacctg tctccggtgt cacgggcatc ctgtgttttg 240 caaacggggc tgacctccct tcctggggag caggaagggt cagggaagga aaagaagtac 300 agaagatctg gctaaacaat ttctgtatgg cgaaagaaaa attctaactt gtacgccctc 360 ttcatgcatc tttaattcaa tttgaatatt ccaggcgaca tcctcactga ccgagcaaag 420 attgacattc gtatcatcac tgtgcaccat tggcttctag gcactccagt ggggtaggag 480 aaggaggtct gaaaccctcg cagagggatc ttgccctcat tctttgggtc tgaaacactg 540 gcagtcgttg gaaacaggac tcagggataa accagcgcaa tggattgggg gacgctgcac 600 actttcatcg ggggtgtcaa caaacactcc accagcatcg ggaaggtgtg gatcacagtc 660 atctttattt tccgagtcat gatcctcgtg gtggctgccc aggaagtgtg gggtgacgag 720 caagaggact tcgtctgcaa cacactgcaa ccgggatgca aaaatgtgtg ctatgaccac 780 tttttcccgg tgtcccacat ccggctgtgg gccctccagc tgatcttcgt ctccacccca 840 gcgctgctgg tggccatgca tgtggcctac tacaggcacg aaaccactcg caagttcagg 900 cgaggagaga agaggaatga tttcaaagac atagaggaca ttaaaaagca gaaggttcgg 960 atagaggggt cgctgtggtg gacgtacacc agcagcatct ttttccgaat catctttgaa 1020 gcagccttta tgtatgtgtt ttacttcctt tacaatgggt accacctgcc ctgggtgttg 1080 aaatgtggga ttgacccctg ccccaacctt gttgactgct ttatttctag gccaacagag 1140 aagaccgtgt ttaccatttt tatgatttct gcgtctgtga tttgcatgct gcttaacgtg 1200 gcagagttgt gctacctgct gctgaaagtg tgttttagga gatcaaagag agcacagacg 1260 caaaaaaatc accccaatca tgccctaaag gagagtaagc agaatgaaat gaatgagctg 1320 atttcagata gtggtcaaaa tgcaatcaca ggttcccaag ctaaacattt caaggtaaaa 1380 tgtagctgcg tcataaggag acttctgtct tctccagaag gcaataccaa cctgaaagtt 1440 ccttctgtag cctgaagagt ttgtaaatga ctttcataat aaatagacac ttgagttaac 1500 tttttgtagg atacttgctc cattcataca caacgtaatc aaatatgtgg tccatctctg 1560 aaaacaagag actgcttgac aaaggagcat tgcagtcact ttgacaggtt ccttttaagt 1620 ggactctctg acaaagtggg tactttctga aaatttatat aactgttgtt gataaggaac 1680 atttatccag gaattgatac gtttattagg aaaagatatt tttataggct tggatgtttt 1740 tagttctgac tttgaattta tataaagtat ttttataatg actggtcttc cttacctgga 1800 aaaacatgcg atgttagttt tagaattaca ccacaagtat ctaaatttgg aacttacaaa 1860 gggtctatct tgtaaatatt gttttgcatt gtctgttggc aaatttgtga actgtcatga 1920 tacgcttaag gtggaaagtg ttcattgcac aatatatttt tactgctttc tgaatgtaga 1980 cggaacagtg tggaagcaga aggctttttt aactcatccg tttgccaatc attgcaaaca 2040 actgaaatgt ggatgtgatt gcctcaataa agctcgtccc cattgcttaa aaaaaaaaa 2099 159 291 PRT Homo sapien 159 Met Asp Trp Gly Thr Leu His Thr Phe Ile Gly Gly Val Asn Lys His 1 5 10 15 Ser Thr Ser Ile Gly Lys Val Trp Ile Thr Val Ile Phe Ile Phe Arg 20 25 30 Val Met Ile Leu Val Val Ala Ala Gln Glu Val Trp Gly Asp Glu Gln 35 40 45 Glu Asp Phe Val Cys Asn Thr Leu Gln Pro Gly Cys Lys Asn Val Cys 50 55 60 Tyr Asp His Phe Phe Pro Val Ser His Ile Arg Leu Trp Ala Leu Gln 65 70 75 80 Leu Ile Phe Val Ser Thr Pro Ala Leu Leu Val Ala Met His Val Ala 85 90 95 Tyr Tyr Arg His Glu Thr Thr Arg Lys Phe Arg Arg Gly Glu Lys Arg 100 105 110 Asn Asp Phe Lys Asp Ile Glu Asp Ile Lys Lys Gln Lys Val Arg Ile 115 120 125 Glu Gly Ser Leu Trp Trp Thr Tyr Thr Ser Ser Ile Phe Phe Arg Ile 130 135 140 Ile Phe Glu Ala Ala Phe Met Tyr Val Phe Tyr Phe Leu Tyr Asn Gly 145 150 155 160 Tyr His Leu Pro Trp Val Leu Lys Cys Gly Ile Asp Pro Cys Pro Asn 165 170 175 Leu Val Asp Cys Phe Ile Ser Arg Pro Thr Glu Lys Thr Val Phe Thr 180 185 190 Ile Phe Met Ile Ser Ala Ser Val Ile Cys Met Leu Leu Asn Val Ala 195 200 205 Glu Leu Cys Tyr Leu Leu Leu Lys Val Cys Phe Arg Arg Ser Lys Arg 210 215 220 Ala Gln Thr Gln Lys Asn His Pro Asn His Ala Leu Lys Glu Ser Lys 225 230 235 240 Gln Asn Glu Met Asn Glu Leu Ile Ser Asp Ser Gly Gln Asn Ala Ile 245 250 255 Thr Gly Ser Gln Ala Lys His Phe Lys Val Lys Cys Ser Cys Val Ile 260 265 270 Arg Arg Leu Leu Ser Ser Pro Glu Gly Asn Thr Asn Leu Lys Val Pro 275 280 285 Ser Val Ala 290 160 3951 DNA Homo sapien 160 tctgcatcca tattgaaaac ctgacacaat gtatgcagca ggctcagtgt gagtgaactg 60 gaggcttctc tacaacatga cccaaaggag cattgcaggt cctatttgca acctgaagtt 120 tgtgactctc ctggttgcct taagttcaga actcccattc ctgggagctg gagtacagct 180 tcaagacaat gggtataatg gattgctcat tgcaattaat cctcaggtac ctgagaatca 240 gaacctcatc tcaaacatta aggaaatgat aactgaagct tcattttacc tatttaatgc 300 taccaagaga agagtatttt tcagaaatat aaagatttta atacctgcca catggaaagc 360 taataataac agcaaaataa aacaagaatc atatgaaaag gcaaatgtca tagtgactga 420 ctggtatggg gcacatggag atgatccata caccctacaa tacagagggt gtggaaaaga 480 gggaaaatac attcatttca cacctaattt cctactgaat gataacttaa cagctggcta 540 cggatcacga ggccgagtgt ttgtccatga atgggcccac ctccgttggg gtgtgttcga 600 tgagtataac aatgacaaac ctttctacat aaatgggcaa aatcaaatta aagtgacaag 660 gtgttcatct gacatcacag gcatttttgt gtgtgaaaaa ggtccttgcc cccaagaaaa 720 ctgtattatt agtaagcttt ttaaagaagg atgcaccttt atctacaata gcacccaaaa 780 tgcaactgca tcaataatgt tcatgcaaag tttatcttct gtggttgaat tttgtaatgc 840 aagtacccac aaccaagaag caccaaacct acagaaccag atgtgcagcc tcagaagtgc 900 atgggatgta atcacagact ctgctgactt tcaccacagc tttcccatga acgggactga 960 gcttccacct cctcccacat tctcgcttgt agaggctggt gacaaagtgg tctgtttagt 1020 gctggatgtg tccagcaaga tggcagaggc tgacagactc cttcaactac aacaagccgc 1080 agaattttat ttgatgcaga ttgttgaaat tcataccttc gtgggcattg ccagtttcga 1140 cagcaaagga gagatcagag cccagctaca ccaaattaac agcaatgatg atcgaaagtt 1200 gctggtttca tatctgccca ccactgtatc agctaaaaca gacatcagca tttgttcagg 1260 gcttaagaaa ggatttgagg tggttgaaaa actgaatgga aaagcttatg gctctgtgat 1320 gatattagtg accagcggag atgataagct tcttggcaat tgcttaccca ctgtgctcag 1380 cagtggttca acaattcact ccattgccct gggttcatct gcagccccaa atctggagga 1440 attatcacgt cttacaggag gtttaaagtt ctttgttcca gatatatcaa actccaatag 1500 catgattgat gctttcagta gaatttcctc tggaactgga gacattttcc agcaacatat 1560 tcagcttgaa agtacaggtg aaaatgtcaa acctcaccat caattgaaaa acacagtgac 1620 tgtggataat actgtgggca acgacactat gtttctagtt acgtggcagg ccagtggtcc 1680 tcctgagatt atattatttg atcctgatgg acgaaaatac tacacaaata attttatcac 1740 caatctaact tttcggacag ctagtctttg gattccagga acagctaagc ctgggcactg 1800 gacttacacc ctgaacaata cccatcattc tctgcaagcc ctgaaagtga cagtgacctc 1860 tcgcgcctcc aactcagctg tgcccccagc cactgtggaa gcctttgtgg aaagagacag 1920 cctccatttt cctcatcctg tgatgattta tgccaatgtg aaacagggat tttatcccat 1980 tcttaatgcc actgtcactg ccacagttga gccagagact ggagatcctg ttacgctgag 2040 actccttgat gatggagcag gtgctgatgt tataaaaaat gatggaattt actcgaggta 2100 ttttttctcc tttgctgcaa atggtagata tagcttgaaa gtgcatgtca atcactctcc 2160 cagcataagc accccagccc actctattcc agggagtcat gctatgtatg taccaggtta 2220 cacagcaaac ggtaatattc agatgaatgc tccaaggaaa tcagtaggca gaaatgagga 2280 ggagcgaaag tggggcttta gccgagtcag ctcaggaggc tccttttcag tgctgggagt 2340 tccagctggc ccccaccctg atgtgtttcc accatgcaaa attattgacc tggaagctgt 2400 aaaagtagaa gaggaattga ccctatcttg gacagcacct ggagaagact ttgatcaggg 2460 ccaggctaca agctatgaaa taagaatgag taaaagtcta cagaatatcc aagatgactt 2520 taacaatgct attttagtaa atacatcaaa gcgaaatcct cagcaagctg gcatcaggga 2580 gatatttacg ttctcacccc aaatttccac gaatggacct gaacatcagc caaatggaga 2640 aacacatgaa agccacagaa tttatgttgc aatacgagca atggatagga actccttaca 2700 gtctgctgta tctaacattg cccaggcgcc tctgtttatt ccccccaatt ctgatcctgt 2760 acctgccaga gattatctta tattgaaagg agttttaaca gcaatgggtt tgataggaat 2820 catttgcctt attatagttg tgacacatca tactttaagc aggaaaaaga gagcagacaa 2880 gaaagagaat ggaacaaaat tattataaat aaatatccaa agtgtcttcc ttcttagata 2940 taagacccat ggccttcgac tacaaaaaca tactaacaaa gtcaaattaa catcaaaact 3000 gtattaaaat gcattgagtt tttgtacaat acagataaga tttttacatg gtagatcaac 3060 aaattctttt tgggggtaga ttagaaaacc cttacacttt ggctatgaac aaataataaa 3120 aattattctt taaagtaatg tctttaaagg caaagggaag ggtaaagtcg gaccagtgtc 3180 aaggaaagtt tgttttattg aggtggaaaa atagccccaa gcagagaaaa ggagggtagg 3240 tctgcattat aactgtctgt gtgaagcaat catttagtta ctttgattaa tttttctttt 3300 ctccttatct gtgcagaaca ggttgcttgt ttacaactga agatcatgct atatttcata 3360 tatgaagccc ctaatgcaaa gctctttacc tcttgctatt ttgttatata tattacagat 3420 gaaatctcac tgctaatgct cagagatctt ttttcactgt aagaggtaac ctttaacaat 3480 atgggtatta cctttgtctc ttcataccgg ttttatgaca aaggtctatt gaatttattt 3540 gtttgtaagt ttctactccc atcaaagcag ctttttaagt tattgccttg gttattatgg 3600 atgatagtta tagcccttat aatgccttaa ctaaggaaga aaagatgtta ttctgagttt 3660 gttttaatac atatatgaac atatagtttt attcaattaa accaaagaag aggtcagcag 3720 ggagatacta acctttggaa atgattagct ggctctgttt tttggttaaa taagagtctt 3780 taatcctttc tccatcaaga gttacttacc aagggcaggg gaagggggat atagaggtcc 3840 caaggaaata aaaatcatct ttcatcttta attttactcc ttcctcttat ttttttaaaa 3900 gattatcgaa caataaaatc atttgccttt ttaattaaaa acataaaaaa a 3951 161 943 PRT Homo sapien 161 Met Thr Gln Arg Ser Ile Ala Gly Pro Ile Cys Asn Leu Lys Phe Val 1 5 10 15 Thr Leu Leu Val Ala Leu Ser Ser Glu Leu Pro Phe Leu Gly Ala Gly 20 25 30 Val Gln Leu Gln Asp Asn Gly Tyr Asn Gly Leu Leu Ile Ala Ile Asn 35 40 45 Pro Gln Val Pro Glu Asn Gln Asn Leu Ile Ser Asn Ile Lys Glu Met 50 55 60 Ile Thr Glu Ala Ser Phe Tyr Leu Phe Asn Ala Thr Lys Arg Arg Val 65 70 75 80 Phe Phe Arg Asn Ile Lys Ile Leu Ile Pro Ala Thr Trp Lys Ala Asn 85 90 95 Asn Asn Ser Lys Ile Lys Gln Glu Ser Tyr Glu Lys Ala Asn Val Ile 100 105 110 Val Thr Asp Trp Tyr Gly Ala His Gly Asp Asp Pro Tyr Thr Leu Gln 115 120 125 Tyr Arg Gly Cys Gly Lys Glu Gly Lys Tyr Ile His Phe Thr Pro Asn 130 135 140 Phe Leu Leu Asn Asp Asn Leu Thr Ala Gly Tyr Gly Ser Arg Gly Arg 145 150 155 160 Val Phe Val His Glu Trp Ala His Leu Arg Trp Gly Val Phe Asp Glu 165 170 175 Tyr Asn Asn Asp Lys Pro Phe Tyr Ile Asn Gly Gln Asn Gln Ile Lys 180 185 190 Val Thr Arg Cys Ser Ser Asp Ile Thr Gly Ile Phe Val Cys Glu Lys 195 200 205 Gly Pro Cys Pro Gln Glu Asn Cys Ile Ile Ser Lys Leu Phe Lys Glu 210 215 220 Gly Cys Thr Phe Ile Tyr Asn Ser Thr Gln Asn Ala Thr Ala Ser Ile 225 230 235 240 Met Phe Met Gln Ser Leu Ser Ser Val Val Glu Phe Cys Asn Ala Ser 245 250 255 Thr His Asn Gln Glu Ala Pro Asn Leu Gln Asn Gln Met Cys Ser Leu 260 265 270 Arg Ser Ala Trp Asp Val Ile Thr Asp Ser Ala Asp Phe His His Ser 275 280 285 Phe Pro Met Asn Gly Thr Glu Leu Pro Pro Pro Pro Thr Phe Ser Leu 290 295 300 Val Glu Ala Gly Asp Lys Val Val Cys Leu Val Leu Asp Val Ser Ser 305 310 315 320 Lys Met Ala Glu Ala Asp Arg Leu Leu Gln Leu Gln Gln Ala Ala Glu 325 330 335 Phe Tyr Leu Met Gln Ile Val Glu Ile His Thr Phe Val Gly Ile Ala 340 345 350 Ser Phe Asp Ser Lys Gly Glu Ile Arg Ala Gln Leu His Gln Ile Asn 355 360 365 Ser Asn Asp Asp Arg Lys Leu Leu Val Ser Tyr Leu Pro Thr Thr Val 370 375 380 Ser Ala Lys Thr Asp Ile Ser Ile Cys Ser Gly Leu Lys Lys Gly Phe 385 390 395 400 Glu Val Val Glu Lys Leu Asn Gly Lys Ala Tyr Gly Ser Val Met Ile 405 410 415 Leu Val Thr Ser Gly Asp Asp Lys Leu Leu Gly Asn Cys Leu Pro Thr 420 425 430 Val Leu Ser Ser Gly Ser Thr Ile His Ser Ile Ala Leu Gly Ser Ser 435 440 445 Ala Ala Pro Asn Leu Glu Glu Leu Ser Arg Leu Thr Gly Gly Leu Lys 450 455 460 Phe Phe Val Pro Asp Ile Ser Asn Ser Asn Ser Met Ile Asp Ala Phe 465 470 475 480 Ser Arg Ile Ser Ser Gly Thr Gly Asp Ile Phe Gln Gln His Ile Gln 485 490 495 Leu Glu Ser Thr Gly Glu Asn Val Lys Pro His His Gln Leu Lys Asn 500 505 510 Thr Val Thr Val Asp Asn Thr Val Gly Asn Asp Thr Met Phe Leu Val 515 520 525 Thr Trp Gln Ala Ser Gly Pro Pro Glu Ile Ile Leu Phe Asp Pro Asp 530 535 540 Gly Arg Lys Tyr Tyr Thr Asn Asn Phe Ile Thr Asn Leu Thr Phe Arg 545 550 555 560 Thr Ala Ser Leu Trp Ile Pro Gly Thr Ala Lys Pro Gly His Trp Thr 565 570 575 Tyr Thr Leu Asn Asn Thr His His Ser Leu Gln Ala Leu Lys Val Thr 580 585 590 Val Thr Ser Arg Ala Ser Asn Ser Ala Val Pro Pro Ala Thr Val Glu 595 600 605 Ala Phe Val Glu Arg Asp Ser Leu His Phe Pro His Pro Val Met Ile 610 615 620 Tyr Ala Asn Val Lys Gln Gly Phe Tyr Pro Ile Leu Asn Ala Thr Val 625 630 635 640 Thr Ala Thr Val Glu Pro Glu Thr Gly Asp Pro Val Thr Leu Arg Leu 645 650 655 Leu Asp Asp Gly Ala Gly Ala Asp Val Ile Lys Asn Asp Gly Ile Tyr 660 665 670 Ser Arg Tyr Phe Phe Ser Phe Ala Ala Asn Gly Arg Tyr Ser Leu Lys 675 680 685 Val His Val Asn His Ser Pro Ser Ile Ser Thr Pro Ala His Ser Ile 690 695 700 Pro Gly Ser His Ala Met Tyr Val Pro Gly Tyr Thr Ala Asn Gly Asn 705 710 715 720 Ile Gln Met Asn Ala Pro Arg Lys Ser Val Gly Arg Asn Glu Glu Glu 725 730 735 Arg Lys Trp Gly Phe Ser Arg Val Ser Ser Gly Gly Ser Phe Ser Val 740 745 750 Leu Gly Val Pro Ala Gly Pro His Pro Asp Val Phe Pro Pro Cys Lys 755 760 765 Ile Ile Asp Leu Glu Ala Val Lys Val Glu Glu Glu Leu Thr Leu Ser 770 775 780 Trp Thr Ala Pro Gly Glu Asp Phe Asp Gln Gly Gln Ala Thr Ser Tyr 785 790 795 800 Glu Ile Arg Met Ser Lys Ser Leu Gln Asn Ile Gln Asp Asp Phe Asn 805 810 815 Asn Ala Ile Leu Val Asn Thr Ser Lys Arg Asn Pro Gln Gln Ala Gly 820 825 830 Ile Arg Glu Ile Phe Thr Phe Ser Pro Gln Ile Ser Thr Asn Gly Pro 835 840 845 Glu His Gln Pro Asn Gly Glu Thr His Glu Ser His Arg Ile Tyr Val 850 855 860 Ala Ile Arg Ala Met Asp Arg Asn Ser Leu Gln Ser Ala Val Ser Asn 865 870 875 880 Ile Ala Gln Ala Pro Leu Phe Ile Pro Pro Asn Ser Asp Pro Val Pro 885 890 895 Ala Arg Asp Tyr Leu Ile Leu Lys Gly Val Leu Thr Ala Met Gly Leu 900 905 910 Ile Gly Ile Ile Cys Leu Ile Ile Val Val Thr His His Thr Leu Ser 915 920 925 Arg Lys Lys Arg Ala Asp Lys Lys Glu Asn Gly Thr Lys Leu Leu 930 935 940 162 498 DNA Homo sapien 162 tggagaacca cgtggacagc accatgaaca tgttgggcgg gggaggcagt gctggccgga 60 agcccctcaa gtcgggtatg aaggagctgg ccgtgttccg ggagaaggtc actgagcagc 120 accggcagat gggcaagggt ggcaagcatc accttggcct ggaggagccc aagaagctgc 180 gaccaccccc tgccaggact ccctgccaac aggaactgga ccaggtcctg gagcggatct 240 ccaccatgcg ccttccggat gagcggggcc ctctggagca cctctactcc ctgcacatcc 300 ccaactgtga caagcatggc ctgtacaacc tcaaacagtg gcaagatgtc tctgaacggg 360 cagcgtgggg agtgctggtg tgtgaacccc aacaccggga agctgatcca gggagccccc 420 accatccggg gggaccccga gtgtcatctc ttctacaatg agcagcagga ggctcgcggg 480 gtgcacaccc cagcggat 498 163 1128 DNA Homo sapien 163 gccacctggc cctcctgatc gacgacacac gcacttgaaa cttgttctca gggtgtgtgg 60 aatcaacttt ccggaagcaa ccagcccacc agaggaggtc ccgagcgcga gcggagacga 120 tgcagcggag actggttcag cagtggagcg tcgcggtgtt cctgctgagc tacgcggtgc 180 cctcctgcgg gcgctcggtg gagggtctca gccgccgcct caaaagagct gtgtctgaac 240 atcagctcct ccatgacaag gggaagtcca tccaagattt acggcgacga ttcttccttc 300 accatctgat cgcagaaatc cacacagctg aaatcagagc tacctcggag gtgtccccta 360 actccaagcc ctctcccaac acaaagaacc accccgtccg atttgggtct gatgatgagg 420 gcagatacct aactcaggaa actaacaagg tggagacgta caaagagcag ccgctcaaga 480 cacctgggaa gaaaaagaaa ggcaagcccg ggaaacgcaa ggagcaggaa aagaaaaaac 540 ggcgaactcg ctctgcctgg ttagactctg gagtgactgg gagtgggcta gaaggggacc 600 acctgtctga cacctccaca acgtcgctgg agctcgattc acggaggcat tgaaattttc 660 agcagagacc ttccaaggac atattgcagg attctgtaat agtgaacata tggaaagtat 720 tagaaatatt tattgtctgt aaatactgta aatgcattgg aataaaactg tctcccccat 780 tgctctatga aactgcacat tggtcattgt gaatattttt ttttttgcca aggctaatcc 840 aattattatt atcacattta ccataattta ttttgtccat tgatgtattt attttgtaaa 900 tgtatcttgg tgctgctgaa tttctatatt ttttgtaaca taatgcactt tagatataca 960 tatcaagtat gttgataaat gacacaatga agtgtctcta ttttgtggtt gattttaatg 1020 aatgcctaaa tataattatc caaattgatt ttcctttgtg catgtaaaaa taacagtatt 1080 ttaaatttgt aaagaatgtc taataaaata taatctaatt acatcatg 1128 164 1310 DNA Homo sapien 164 gggcctggtt cgcaaagaag ctgacttcag agggggaaac tttcttcttt taggaggcgg 60 ttagccctgt tccacgaacc caggagaact gctggccaga ttaattagac attgctatgg 120 gagacgtgta aacacactac ttatcattga tgcatatata aaaccatttt attttcgcta 180 ttatttcaga ggaagcgcct ctgatttgtt tcttttttcc ctttttgctc tttctggctg 240 tgtggtttgg agaaagcaca gttggagtag ccggttgcta aataagtccc gagcgcgagc 300 ggagacgatg cagcggagac tggttcagca gtggagcgtc gcggtgttcc tgctgagcta 360 cgcggtgccc tcctgcgggc gctcggtgga gggtctcagc cgccgcctca aaagagctgt 420 gtctgaacat cagctcctcc atgacaaggg gaagtccatc caagatttac ggcgacgatt 480 cttccttcac catctgatcg cagaaatcca cacagctgaa atcagagcta cctcggaggt 540 gtcccctaac tccaagccct ctcccaacac aaagaaccac cccgtccgat ttgggtctga 600 tgatgagggc agatacctaa ctcaggaaac taacaaggtg gagacgtaca aagagcagcc 660 gctcaagaca cctgggaaga aaaagaaagg caagcccggg aaacgcaagg agcaggaaaa 720 gaaaaaacgg cgaactcgct ctgcctggtt agactctgga gtgactggga gtgggctaga 780 aggggaccac ctgtctgaca cctccacaac gtcgctggag ctcgattcac ggaggcattg 840 aaattttcag cagagacctt ccaaggacat attgcaggat tctgtaatag tgaacatatg 900 gaaagtatta gaaatattta ttgtctgtaa atactgtaaa tgcattggaa taaaactgtc 960 tcccccattg ctctatgaaa ctgcacattg gtcattgtga atattttttt ttttgccaag 1020 gctaatccaa ttattattat cacatttacc ataatttatt ttgtccattg atgtatttat 1080 tttgtaaatg tatcttggtg ctgctgaatt tctatatttt ttgtaacata atgcacttta 1140 gatatacata tcaagtatgt tgataaatga cacaatgaag tgtctctatt ttgtggttga 1200 ttttaatgaa tgcctaaata taattatcca aattgatttt cctttgtgcc cgtaaaaata 1260 acagtatttt aaatttgtaa agaatgtcta ataaaatata atctaattac 1310 165 177 PRT Homo sapien 165 Met Gln Arg Arg Leu Val Gln Gln Trp Ser Val Ala Val Phe Leu Leu 1 5 10 15 Ser Tyr Ala Val Pro Ser Cys Gly Arg Ser Val Glu Gly Leu Ser Arg 20 25 30 Arg Leu Lys Arg Ala Val Ser Glu His Gln Leu Leu His Asp Lys Gly 35 40 45 Lys Ser Ile Gln Asp Leu Arg Arg Arg Phe Phe Leu His His Leu Ile 50 55 60 Ala Glu Ile His Thr Ala Glu Ile Arg Ala Thr Ser Glu Val Ser Pro 65 70 75 80 Asn Ser Lys Pro Ser Pro Asn Thr Lys Asn His Pro Val Arg Phe Gly 85 90 95 Ser Asp Asp Glu Gly Arg Tyr Leu Thr Gln Glu Thr Asn Lys Val Glu 100 105 110 Thr Tyr Lys Glu Gln Pro Leu Lys Thr Pro Gly Lys Lys Lys Lys Gly 115 120 125 Lys Pro Gly Lys Arg Lys Glu Gln Glu Lys Lys Lys Arg Arg Thr Arg 130 135 140 Ser Ala Trp Leu Asp Ser Gly Val Thr Gly Ser Gly Leu Glu Gly Asp 145 150 155 160 His Leu Ser Asp Thr Ser Thr Thr Ser Leu Glu Leu Asp Ser Arg Arg 165 170 175 His 166 177 PRT Homo sapien 166 Met Gln Arg Arg Leu Val Gln Gln Trp Ser Val Ala Val Phe Leu Leu 1 5 10 15 Ser Tyr Ala Val Pro Ser Cys Gly Arg Ser Val Glu Gly Leu Ser Arg 20 25 30 Arg Leu Lys Arg Ala Val Ser Glu His Gln Leu Leu His Asp Lys Gly 35 40 45 Lys Ser Ile Gln Asp Leu Arg Arg Arg Phe Phe Leu His His Leu Ile 50 55 60 Ala Glu Ile His Thr Ala Glu Ile Arg Ala Thr Ser Glu Val Ser Pro 65 70 75 80 Asn Ser Lys Pro Ser Pro Asn Thr Lys Asn His Pro Val Arg Phe Gly 85 90 95 Ser Asp Asp Glu Gly Arg Tyr Leu Thr Gln Glu Thr Asn Lys Val Glu 100 105 110 Thr Tyr Lys Glu Gln Pro Leu Lys Thr Pro Gly Lys Lys Lys Lys Gly 115 120 125 Lys Pro Gly Lys Arg Lys Glu Gln Glu Lys Lys Lys Arg Arg Thr Arg 130 135 140 Ser Ala Trp Leu Asp Ser Gly Val Thr Gly Ser Gly Leu Glu Gly Asp 145 150 155 160 His Leu Ser Asp Thr Ser Thr Thr Ser Leu Glu Leu Asp Ser Arg Arg 165 170 175 His 167 3362 DNA Homo sapien 167 cacaatgtat gcagcaggct cagtgtgagt gaactggagg cttctctaca acatgaccca 60 aaggagcatt gcaggtccta tttgcaacct gaagtttgtg actctcctgg ttgccttaag 120 ttcagaactc ccattcctgg gagctggagt acagcttcaa gacaatgggt ataatggatt 180 gctcattgca attaatcctc aggtacctga gaatcagaac ctcatctcaa acattaagga 240 aatgataact gaagcttcat tttacctatt taatgctacc aagagaagag tatttttcag 300 aaatataaag attttaatac ctgccacatg gaaagctaat aataacagca aaataaaaca 360 agaatcatat gaaaaggcaa atgtcatagt gactgactgg tatggggcac atggagatga 420 tccatacacc ctacaataca gagggtgtgg aaaagaggga aaatacattc atttcacacc 480 taatttccta ctgaatgata acttaacagc tggctacgga tcacgaggcc gagtgtttgt 540 ccatgaatgg gcccacctcc gttggggtgt gttcgatgag tataacaatg acaaaccttt 600 ctacataaat gggcaaaatc aaattaaagt gacaaggtgt tcatctgaca tcacaggcat 660 ttttgtgtgt gaaaaaggtc cttgccccca agaaaactgt attattagta agctttttaa 720 agaaggatgc acctttatct acaatagcac ccaaaatgca actgcatcaa taatgttcat 780 gcaaagttta tcttctgtgg ttgaattttg taatgcaagt acccacaacc aagaagcacc 840 aaacctacag aaccagatgt gcagcctcag aagtgcatgg gatgtaatca cagactctgc 900 tgactttcac cacagctttc ccatgaacgg gactgagctt ccacctcctc ccacattctc 960 gcttgtagag gctggtgaca aagtggtctg tttagtgctg gatgtgtcca gcaagatggc 1020 agaggctgac agactccttc aactacaaca agccgcagaa ttttatttga tgcagattgt 1080 tgaaattcat accttcgtgg gcattgccag tttcgacagc aaaggagaga tcagagccca 1140 gctacaccaa attaacagca atgatgatcg aaagttgctg gtttcatatc tgcccaccac 1200 tgtatcagct aaaacagaca tcagcatttg ttcagggctt aagaaaggat ttgaggtggt 1260 tgaaaaactg aatggaaaag cttatggctc tgtgatgata ttagtgacca gcggagatga 1320 taagcttctt ggcaattgct tacccactgt gctcagcagt ggttcaacaa ttcactccat 1380 tgccctgggt tcatctgcag ccccaaatct ggaggaatta tcacgtctta caggaggttt 1440 aaagttcttt gttccagata tatcaaactc caatagcatg attgatgctt tcagtagaat 1500 ttcctctgga actggagaca ttttccagca acatattcag cttgaaagta caggtgaaaa 1560 tgtcaaacct caccatcaat tgaaaaacac agtgactgtg gataatactg tgggcaacga 1620 cactatgttt ctagttacgt ggcaggccag tggtcctcct gagattatat tatttgatcc 1680 tgatggacga aaatactaca caaataattt tatcaccaat ctaacttttc ggacagctag 1740 tctttggatt ccaggaacag ctaagcctgg gcactggact tacaccctga tgtgtttcca 1800 ccatgcaaaa ttattgacct ggaagctgta aaagtagaag aggaattgac cctatcttgg 1860 acagcacctg gagaagactt tgatcagggc caggctacaa gctatgaaat aagaatgagt 1920 aaaagtctac agaatatcca agatgacttt aacaatgcta ttttagtaaa tacatcaaag 1980 cgaaatcctc agcaagctgg catcagggag atatttacgt tctcacccca aatttccacg 2040 aatggacctg aacatcagcc aaatggagaa acacatgaaa gccacagaat ttatgttgca 2100 atacgagcaa tggataggaa ctccttacag tctgctgtat ctaacattgc ccaggcgcct 2160 ctgtttattc cccccaattc tgatcctgta cctgccagag attatcttat attgaaagga 2220 gttttaacag caatgggttt gataggaatc atttgcctta ttatagttgt gacacatcat 2280 actttaagca ggaaaaagag agcagacaag aaagagaatg gaacaaaatt attataaata 2340 aatatccaaa gtgtcttcct tcttagatat aagacccatg gccttcgact acaaaaacat 2400 actaacaaag tcaaattaac atcaaaactg tattaaaatg cattgagttt ttgtacaata 2460 cagataagat ttttacatgg tagatcaaca aattcttttt gggggtagat tagaaaaccc 2520 ttacactttg gctatgaaca aataataaaa attattcttt aaagtaatgt ctttaaaggc 2580 aaagggaagg gtaaagtcgg accagtgtca aggaaagttt gttttattga ggtggaaaaa 2640 tagccccaag cagagaaaag gagggtaggt ctgcattata actgtctgtg tgaagcaatc 2700 atttagttac tttgattaat ttttcttttc tccttatctg tgcagaacag gttgcttgtt 2760 tacaactgaa gatcatgcta tatttcatat atgaagcccc taatgcaaag ctctttacct 2820 cttgctattt tgttatatat attacagatg aaatctcact gctaatgctc agagatcttt 2880 tttcactgta agaggtaacc tttaacaata tgggtattac ctttgtctct tcataccggt 2940 tttatgacaa aggtctattg aatttatttg tttgtaagtt tctactccca tcaaagcagc 3000 tttctaagtt attgccttgg ttattatgga tgatagttat agcccttata atgccttaac 3060 taaggaagaa aagatgttat tctgagtttg ttttaataca tatatgaaca tatagtttta 3120 ttcaattaaa ccaaagaaga ggtcagcagg gagatactaa cctttggaaa tgattagctg 3180 gctctgtttt ttggttaaat aagagtcttt aatcctttct ccatcaagag ttacttacca 3240 agggcagggg aagggggata tagaggtcac aaggaaataa aaatcatctt tcatctttaa 3300 ttttactcct tcctcttatt tttttaaaag attatcgaac aataaaatca tttgcctttt 3360 tt 3362 168 2784 DNA Homo sapien 168 tctgcatcca tattgaaaac ctgacacaat gtatgcagca ggctcagtgt gagtgaactg 60 gaggcttctc tacaacatga cccaaaggag cattgcaggt cctatttgca acctgaagtt 120 tgtgactctc ctggttgcct taagttcaga actcccattc ctgggagctg gagtacagct 180 tcaagacaat gggtataatg gattgctcat tgcaattaat cctcaggtac ctgagaatca 240 gaacctcatc tcaaacatta aggaaatgat aactgaagct tcattttacc tatttaatgc 300 taccaagaga agagtatttt tcagaaatat aaagatttta atacctgcca catggaaagc 360 taataataac agcaaaataa aacaagaatc atatgaaaag gcaaatgtca tagtgactga 420 ctggtatggg gcacatggag atgatccata caccctacaa tacagagggt gtggaaaaga 480 gggaaaatac attcatttca cacctaattt cctactgaat gataacttaa cagctggcta 540 cggatcacga ggccgagtgt ttgtccatga atgggcccac ctccgttggg gtgtgttcga 600 tgagtataac aatgacaaac ctttctacat aaatgggcaa aatcaaatta aagtgacaag 660 gtgttcatct gacatcacag gcatttttgt gtgtgaaaaa ggtccttgcc cccaagaaaa 720 ctgtattatt agtaagcttt ttaaagaagg atgcaccttt atctacaata gcacccaaaa 780 tgcaactgca tcaataatgt tcatgcaaag tttatcttct gtggttgaat tttgtaatgc 840 aagtacccac aaccaagaag caccaaacct acagaaccag atgtgcagcc tcagaagtgc 900 atgggatgta atcacagact ctgctgactt tcaccacagc tttcccatga acgggactga 960 gcttccacct cctcccacat tctcgcttgt agaggctggt gacaaagtgg tctgtttagt 1020 gctggatgtg tccagcaaga tggcagaggc tgacagactc cttcaactac aacaagccgc 1080 agaattttat ttgatgcaga ttgttgaaat tcataccttc gtgggcattg ccagtttcga 1140 cagcaaagga gagatcagag cccagctaca ccaaattaac agcaatgatg atcgaaagtt 1200 gctggtttca tatctgccca ccactgtatc agctaaaaca gacatcagca tttgttcagg 1260 gcttaagaaa ggatttgagg tggttgaaaa actgaatgga aaagcttatg gctctgtgat 1320 gatattagtg accagcggag atgataagct tcttggcaat tgcttaccca ctgtgctcag 1380 cagtggttca acaattcact ccattgccct gggttcatct gcagccccaa atctggagga 1440 attatcacgt cttacaggag gtttaaagtt ctttgttcca gatatatcaa actccaatag 1500 catgattgat gctttcagta gaatttcctc tggaactgga gacattttcc agcaacatat 1560 tcagcttgaa agtacaggtg aaaatgtcaa acctcaccat caattgaaaa acacagtgac 1620 tgtggataat actgtgggca acgacactat gtttctagtt acgtggcagg ccagtggtcc 1680 tcctgagatt atattatttg atcctgatgg acgaaaatac tacacaaata attttatcac 1740 caatctaact tttcggacag ctagtctttg gattccagga acagctaagc ctgggcactg 1800 gacttacacc ctgaacaata cccatcattc tctgcaagcc ctgaaagtga cagtgacctc 1860 tcgcgcctcc aactcagctg tgcccccagc cactgtggaa gcctttgtgg aaagagacag 1920 cctccatttt cctcatcctg tgatgattta tgccaatgtg aaacagggat tttatcccat 1980 tcttaatgcc actgtcactg ccacagttga gccagagact ggagatcctg ttacgctgag 2040 actccttgat gatggagcag gtgctgatgt tataaaaaat gatggaattt actcgaggta 2100 ttttttctcc tttgctgcaa atggtagata tagcttgaaa gtgcatgtca atcactctcc 2160 cagcataagc accccagccc actctattcc agggagtcat gctatgtatg taccaggtta 2220 cacagcaaac ggtaatattc agatgaatgc tccaaggaaa tcagtaggca gaaatgagga 2280 ggagcgaaag tggggcttta gccgagtcag ctcaggaggc tccttttcag tgctgggagt 2340 tccagctggc ccccaccctg atgtgtttcc accatgcaaa attattgacc tggaagctgt 2400 aaatagaaga ggaattgacc ctatcttgga cagcacctgg agaagacttt gatcagggcc 2460 aggctacaag ctatgaaata agaatgagta aaagtctaca gaatatccaa gatgacttta 2520 acaatgctat tttagtaaat acatcaaagc gaaatcctca gcaagctggc atcagggaga 2580 tatttacgtt ctcaccccaa atttccacga atggacctga acatcagcca aatggagaaa 2640 cacatgaaag ccacagaatt tatgttgcaa tacgagcaat ggataggaac tccttacagt 2700 ctgctgtatc taacattgcc caggcgcctc tgtttattcc ccccaattct gatcctgtac 2760 ctgccagaga ttatcttata ttga 2784 169 592 PRT Homo sapien 169 Met Thr Gln Arg Ser Ile Ala Gly Pro Ile Cys Asn Leu Lys Phe Val 1 5 10 15 Thr Leu Leu Val Ala Leu Ser Ser Glu Leu Pro Phe Leu Gly Ala Gly 20 25 30 Val Gln Leu Gln Asp Asn Gly Tyr Asn Gly Leu Leu Ile Ala Ile Asn 35 40 45 Pro Gln Val Pro Glu Asn Gln Asn Leu Ile Ser Asn Ile Lys Glu Met 50 55 60 Ile Thr Glu Ala Ser Phe Tyr Leu Phe Asn Ala Thr Lys Arg Arg Val 65 70 75 80 Phe Phe Arg Asn Ile Lys Ile Leu Ile Pro Ala Thr Trp Lys Ala Asn 85 90 95 Asn Asn Ser Lys Ile Lys Gln Glu Ser Tyr Glu Lys Ala Asn Val Ile 100 105 110 Val Thr Asp Trp Tyr Gly Ala His Gly Asp Asp Pro Tyr Thr Leu Gln 115 120 125 Tyr Arg Gly Cys Gly Lys Glu Gly Lys Tyr Ile His Phe Thr Pro Asn 130 135 140 Phe Leu Leu Asn Asp Asn Leu Thr Ala Gly Tyr Gly Ser Arg Gly Arg 145 150 155 160 Val Phe Val His Glu Trp Ala His Leu Arg Trp Gly Val Phe Asp Glu 165 170 175 Tyr Asn Asn Asp Lys Pro Phe Tyr Ile Asn Gly Gln Asn Gln Ile Lys 180 185 190 Val Thr Arg Cys Ser Ser Asp Ile Thr Gly Ile Phe Val Cys Glu Lys 195 200 205 Gly Pro Cys Pro Gln Glu Asn Cys Ile Ile Ser Lys Leu Phe Lys Glu 210 215 220 Gly Cys Thr Phe Ile Tyr Asn Ser Thr Gln Asn Ala Thr Ala Ser Ile 225 230 235 240 Met Phe Met Gln Ser Leu Ser Ser Val Val Glu Phe Cys Asn Ala Ser 245 250 255 Thr His Asn Gln Glu Ala Pro Asn Leu Gln Asn Gln Met Cys Ser Leu 260 265 270 Arg Ser Ala Trp Asp Val Ile Thr Asp Ser Ala Asp Phe His His Ser 275 280 285 Phe Pro Met Asn Gly Thr Glu Leu Pro Pro Pro Pro Thr Phe Ser Leu 290 295 300 Val Glu Ala Gly Asp Lys Val Val Cys Leu Val Leu Asp Val Ser Ser 305 310 315 320 Lys Met Ala Glu Ala Asp Arg Leu Leu Gln Leu Gln Gln Ala Ala Glu 325 330 335 Phe Tyr Leu Met Gln Ile Val Glu Ile His Thr Phe Val Gly Ile Ala 340 345 350 Ser Phe Asp Ser Lys Gly Glu Ile Arg Ala Gln Leu His Gln Ile Asn 355 360 365 Ser Asn Asp Asp Arg Lys Leu Leu Val Ser Tyr Leu Pro Thr Thr Val 370 375 380 Ser Ala Lys Thr Asp Ile Ser Ile Cys Ser Gly Leu Lys Lys Gly Phe 385 390 395 400 Glu Val Val Glu Lys Leu Asn Gly Lys Ala Tyr Gly Ser Val Met Ile 405 410 415 Leu Val Thr Ser Gly Asp Asp Lys Leu Leu Gly Asn Cys Leu Pro Thr 420 425 430 Val Leu Ser Ser Gly Ser Thr Ile His Ser Ile Ala Leu Gly Ser Ser 435 440 445 Ala Ala Pro Asn Leu Glu Glu Leu Ser Arg Leu Thr Gly Gly Leu Lys 450 455 460 Phe Phe Val Pro Asp Ile Ser Asn Ser Asn Ser Met Ile Asp Ala Phe 465 470 475 480 Ser Arg Ile Ser Ser Gly Thr Gly Asp Ile Phe Gln Gln His Ile Gln 485 490 495 Leu Glu Ser Thr Gly Glu Asn Val Lys Pro His His Gln Leu Lys Asn 500 505 510 Thr Val Thr Val Asp Asn Thr Val Gly Asn Asp Thr Met Phe Leu Val 515 520 525 Thr Trp Gln Ala Ser Gly Pro Pro Glu Ile Ile Leu Phe Asp Pro Asp 530 535 540 Gly Arg Lys Tyr Tyr Thr Asn Asn Phe Ile Thr Asn Leu Thr Phe Arg 545 550 555 560 Thr Ala Ser Leu Trp Ile Pro Gly Thr Ala Lys Pro Gly His Trp Thr 565 570 575 Tyr Thr Leu Met Cys Phe His His Ala Lys Leu Leu Thr Trp Lys Leu 580 585 590 170 791 PRT Homo sapien 170 Met Thr Gln Arg Ser Ile Ala Gly Pro Ile Cys Asn Leu Lys Phe Val 1 5 10 15 Thr Leu Leu Val Ala Leu Ser Ser Glu Leu Pro Phe Leu Gly Ala Gly 20 25 30 Val Gln Leu Gln Asp Asn Gly Tyr Asn Gly Leu Leu Ile Ala Ile Asn 35 40 45 Pro Gln Val Pro Glu Asn Gln Asn Leu Ile Ser Asn Ile Lys Glu Met 50 55 60 Ile Thr Glu Ala Ser Phe Tyr Leu Phe Asn Ala Thr Lys Arg Arg Val 65 70 75 80 Phe Phe Arg Asn Ile Lys Ile Leu Ile Pro Ala Thr Trp Lys Ala Asn 85 90 95 Asn Asn Ser Lys Ile Lys Gln Glu Ser Tyr Glu Lys Ala Asn Val Ile 100 105 110 Val Thr Asp Trp Tyr Gly Ala His Gly Asp Asp Pro Tyr Thr Leu Gln 115 120 125 Tyr Arg Gly Cys Gly Lys Glu Gly Lys Tyr Ile His Phe Thr Pro Asn 130 135 140 Phe Leu Leu Asn Asp Asn Leu Thr Ala Gly Tyr Gly Ser Arg Gly Arg 145 150 155 160 Val Phe Val His Glu Trp Ala His Leu Arg Trp Gly Val Phe Asp Glu 165 170 175 Tyr Asn Asn Asp Lys Pro Phe Tyr Ile Asn Gly Gln Asn Gln Ile Lys 180 185 190 Val Thr Arg Cys Ser Ser Asp Ile Thr Gly Ile Phe Val Cys Glu Lys 195 200 205 Gly Pro Cys Pro Gln Glu Asn Cys Ile Ile Ser Lys Leu Phe Lys Glu 210 215 220 Gly Cys Thr Phe Ile Tyr Asn Ser Thr Gln Asn Ala Thr Ala Ser Ile 225 230 235 240 Met Phe Met Gln Ser Leu Ser Ser Val Val Glu Phe Cys Asn Ala Ser 245 250 255 Thr His Asn Gln Glu Ala Pro Asn Leu Gln Asn Gln Met Cys Ser Leu 260 265 270 Arg Ser Ala Trp Asp Val Ile Thr Asp Ser Ala Asp Phe His His Ser 275 280 285 Phe Pro Met Asn Gly Thr Glu Leu Pro Pro Pro Pro Thr Phe Ser Leu 290 295 300 Val Glu Ala Gly Asp Lys Val Val Cys Leu Val Leu Asp Val Ser Ser 305 310 315 320 Lys Met Ala Glu Ala Asp Arg Leu Leu Gln Leu Gln Gln Ala Ala Glu 325 330 335 Phe Tyr Leu Met Gln Ile Val Glu Ile His Thr Phe Val Gly Ile Ala 340 345 350 Ser Phe Asp Ser Lys Gly Glu Ile Arg Ala Gln Leu His Gln Ile Asn 355 360 365 Ser Asn Asp Asp Arg Lys Leu Leu Val Ser Tyr Leu Pro Thr Thr Val 370 375 380 Ser Ala Lys Thr Asp Ile Ser Ile Cys Ser Gly Leu Lys Lys Gly Phe 385 390 395 400 Glu Val Val Glu Lys Leu Asn Gly Lys Ala Tyr Gly Ser Val Met Ile 405 410 415 Leu Val Thr Ser Gly Asp Asp Lys Leu Leu Gly Asn Cys Leu Pro Thr 420 425 430 Val Leu Ser Ser Gly Ser Thr Ile His Ser Ile Ala Leu Gly Ser Ser 435 440 445 Ala Ala Pro Asn Leu Glu Glu Leu Ser Arg Leu Thr Gly Gly Leu Lys 450 455 460 Phe Phe Val Pro Asp Ile Ser Asn Ser Asn Ser Met Ile Asp Ala Phe 465 470 475 480 Ser Arg Ile Ser Ser Gly Thr Gly Asp Ile Phe Gln Gln His Ile Gln 485 490 495 Leu Glu Ser Thr Gly Glu Asn Val Lys Pro His His Gln Leu Lys Asn 500 505 510 Thr Val Thr Val Asp Asn Thr Val Gly Asn Asp Thr Met Phe Leu Val 515 520 525 Thr Trp Gln Ala Ser Gly Pro Pro Glu Ile Ile Leu Phe Asp Pro Asp 530 535 540 Gly Arg Lys Tyr Tyr Thr Asn Asn Phe Ile Thr Asn Leu Thr Phe Arg 545 550 555 560 Thr Ala Ser Leu Trp Ile Pro Gly Thr Ala Lys Pro Gly His Trp Thr 565 570 575 Tyr Thr Leu Asn Asn Thr His His Ser Leu Gln Ala Leu Lys Val Thr 580 585 590 Val Thr Ser Arg Ala Ser Asn Ser Ala Val Pro Pro Ala Thr Val Glu 595 600 605 Ala Phe Val Glu Arg Asp Ser Leu His Phe Pro His Pro Val Met Ile 610 615 620 Tyr Ala Asn Val Lys Gln Gly Phe Tyr Pro Ile Leu Asn Ala Thr Val 625 630 635 640 Thr Ala Thr Val Glu Pro Glu Thr Gly Asp Pro Val Thr Leu Arg Leu 645 650 655 Leu Asp Asp Gly Ala Gly Ala Asp Val Ile Lys Asn Asp Gly Ile Tyr 660 665 670 Ser Arg Tyr Phe Phe Ser Phe Ala Ala Asn Gly Arg Tyr Ser Leu Lys 675 680 685 Val His Val Asn His Ser Pro Ser Ile Ser Thr Pro Ala His Ser Ile 690 695 700 Pro Gly Ser His Ala Met Tyr Val Pro Gly Tyr Thr Ala Asn Gly Asn 705 710 715 720 Ile Gln Met Asn Ala Pro Arg Lys Ser Val Gly Arg Asn Glu Glu Glu 725 730 735 Arg Lys Trp Gly Phe Ser Arg Val Ser Ser Gly Gly Ser Phe Ser Val 740 745 750 Leu Gly Val Pro Ala Gly Pro His Pro Asp Val Phe Pro Pro Cys Lys 755 760 765 Ile Ile Asp Leu Glu Ala Val Asn Arg Arg Gly Ile Asp Pro Ile Leu 770 775 780 Asp Ser Thr Trp Arg Arg Leu 785 790 171 1491 DNA Homo sapien 171 cctcctgcca gccaagtgaa gacatgctta cttccccttc accttccttc atgatgtggg 60 aagagtgctg caacccagcc ctagccaacg ccgcatgaga gggagtgtgc cgagggcttc 120 tgagaaggtt tctctcacat ctagaaagaa gcgcttaaga tgtggcagcc cctcttcttc 180 aagtggctct tgtcctgttg ccctgggagt tctcaaattg ctgcagcagc ctccacccag 240 cctgaggatg acatcaatac acagaggaag aagagtcagg aaaagatgag agaagttaca 300 gactctcctg ggcgaccccg agagcttacc attcctcaga cttcttcaca tggtgctaac 360 agatttgttc ctaaaagtaa agctctagag gccgtcaaat tggcaataga agccgggttc 420 caccatattg attctgcaca tgtttacaat aatgaggagc aggttggact ggccatccga 480 agcaagattg cagatggcag tgtgaagaga gaagacatat tctacacttc aaagctttgg 540 agcaattccc atcgaccaga gttggtccga ccagccttgg aaaggtcact gaaaaatctt 600 caattggact atgttgacct ctatcttatt cattttccag tgtctgtaaa gccaggtgag 660 gaagtgatcc caaaagatga aaatggaaaa atactatttg acacagtgga tctctgtgcc 720 acatgggagg ccatggagaa gtgtaaagat gcaggattgg ccaagtccat cggggtgtcc 780 aacttcaacc acaggctgct ggagatgatc ctcaacaagc cagggctcaa gtacaagcct 840 gtctgcaacc aggtggaatg tcatccttac ttcaaccaga gaaaactgct ggatttctgc 900 aagtcaaaag acattgttct ggttgcctat agtgctctgg gatcccatcg agaagaacca 960 tgggtggacc cgaactcccc ggtgctcttg gaggacccag tcctttgtgc cttggcaaaa 1020 aagcacaagc gaaccccagc cctgattgcc ctgcgctacc agctgcagcg tggggttgtg 1080 gtcctggcca agagctacaa tgagcagcgc atcagacaga acgtgcaggt gtttgaattc 1140 cagttgactt cagaggagat gaaagccata gatggcctaa acagaaatgt gcgatatttg 1200 acccttgata tttttgctgg cccccctaat tatccatttt ctgatgaata ttaacatgga 1260 gggcattgca tgaggtctgc cagaaggccc tgcgtgtgga tggtgacaca gaggatggct 1320 ctatgctggt gactggacac atcgcctctg gttaaatctc tcctgcttgg cgacttcagt 1380 aagctacagc taagcccatc ggccggaaaa gaaagacaat aattttgttt ttcattttga 1440 aaaaattaaa tgctctctcc taaagattct tcacctaaaa aaaaaaaaaa a 1491 172 364 PRT Homo sapien 172 Met Trp Gln Pro Leu Phe Phe Lys Trp Leu Leu Ser Cys Cys Pro Gly 1 5 10 15 Ser Ser Gln Ile Ala Ala Ala Ala Ser Thr Gln Pro Glu Asp Asp Ile 20 25 30 Asn Thr Gln Arg Lys Lys Ser Gln Glu Lys Met Arg Glu Val Thr Asp 35 40 45 Ser Pro Gly Arg Pro Arg Glu Leu Thr Ile Pro Gln Thr Ser Ser His 50 55 60 Gly Ala Asn Arg Phe Val Pro Lys Ser Lys Ala Leu Glu Ala Val Lys 65 70 75 80 Leu Ala Ile Glu Ala Gly Phe His His Ile Asp Ser Ala His Val Tyr 85 90 95 Asn Asn Glu Glu Gln Val Gly Leu Ala Ile Arg Ser Lys Ile Ala Asp 100 105 110 Gly Ser Val Lys Arg Glu Asp Ile Phe Tyr Thr Ser Lys Leu Trp Ser 115 120 125 Asn Ser His Arg Pro Glu Leu Val Arg Pro Ala Leu Glu Arg Ser Leu 130 135 140 Lys Asn Leu Gln Leu Asp Tyr Val Asp Leu Tyr Leu Ile His Phe Pro 145 150 155 160 Val Ser Val Lys Pro Gly Glu Glu Val Ile Pro Lys Asp Glu Asn Gly 165 170 175 Lys Ile Leu Phe Asp Thr Val Asp Leu Cys Ala Thr Trp Glu Ala Met 180 185 190 Glu Lys Cys Lys Asp Ala Gly Leu Ala Lys Ser Ile Gly Val Ser Asn 195 200 205 Phe Asn His Arg Leu Leu Glu Met Ile Leu Asn Lys Pro Gly Leu Lys 210 215 220 Tyr Lys Pro Val Cys Asn Gln Val Glu Cys His Pro Tyr Phe Asn Gln 225 230 235 240 Arg Lys Leu Leu Asp Phe Cys Lys Ser Lys Asp Ile Val Leu Val Ala 245 250 255 Tyr Ser Ala Leu Gly Ser His Arg Glu Glu Pro Trp Val Asp Pro Asn 260 265 270 Ser Pro Val Leu Leu Glu Asp Pro Val Leu Cys Ala Leu Ala Lys Lys 275 280 285 His Lys Arg Thr Pro Ala Leu Ile Ala Leu Arg Tyr Gln Leu Gln Arg 290 295 300 Gly Val Val Val Leu Ala Lys Ser Tyr Asn Glu Gln Arg Ile Arg Gln 305 310 315 320 Asn Val Gln Val Phe Glu Phe Gln Leu Thr Ser Glu Glu Met Lys Ala 325 330 335 Ile Asp Gly Leu Asn Arg Asn Val Arg Tyr Leu Thr Leu Asp Ile Phe 340 345 350 Ala Gly Pro Pro Asn Tyr Pro Phe Ser Asp Glu Tyr 355 360 173 1988 DNA Homo sapiens 173 cgggagccgc ctccccgcgg cctcttcgct tttgtggcgg cgcccgcgct cgcaggccac 60 tctctgctgt cgcccgtccc gcgcgctcct ccgacccgct ccgctccgct ccgctcggcc 120 ccgcgccgcc cgtcaacatg atccgctgcg gcctggcctg cgagcgctgc cgctggatcc 180 tgcccctgct cctactcagc gccatcgcct tcgacatcat cgcgctggcc ggccgcggct 240 ggttgcagtc tagcgaccac ggccagacgt cctcgctgtg gtggaaatgc tcccaagagg 300 gcggcggcag cgggtcctac gaggagggct gtcagagcct catggagtac gcgtggggta 360 gagcagcggc tgccatgctc ttctgtggct tcatcatcct ggtgatctgt ttcatcctct 420 ccttcttcgc cctctgtgga ccccagatgc ttgtcttcct gagagtgatt ggaggtctcc 480 ttgccttggc tgctgtgttc cagatcatct ccctggtaat ttaccccgtg aagtacaccc 540 agaccttcac ccttcatgcc aaccctgctg tcacttacat ctataactgg gcctacggct 600 ttgggtgggc agccacgatt atcctgatcg gctgtgcctt cttcttctgc tgcctcccca 660 actacgaaga tgaccttctg ggcaatgcca agcccaggta cttctacaca tctgcctaac 720 ttgggaatga atgtgggaga aaatcgctgc tgctgagatg gactccagaa gaagaaactg 780 tttctccagg cgactttgaa cccatttttt ggcagtgttc atattattaa actagtcaaa 840 aatgctaaaa taatttggga gaaaatattt tttaagtagt gttatagttt catgtttatc 900 ttttattatg ttttgtgaag ttgtgtcttt tcactaatta cctatactat gccaatattt 960 ccttatatct atccataaca tttatactac atttgtaaga gaatatgcac gtgaaactta 1020 acactttata aggtaaaaat gaggtttcca agatttaata atctgatcaa gttcttgtta 1080 tttccaaata gaatggactt ggtctgttaa gggctaagga gaagaggaag ataaggttaa 1140 aagttgttaa tgaccaaaca ttctaaaaga aatgcaaaaa aaaagtttat tttcaagcct 1200 tcgaactatt taaggaaagc aaaatcattt cctaaatgca tatcatttgt gagaatttct 1260 cattaatatc ctgaatcatt catttcagct aaggcttcat gttgactcga tatgtcatct 1320 aggaaagtac tatttcatgg tccaaacctg ttgccatagt tggtaaggct ttcctttaag 1380 tgtgaaatat ttagatgaaa ttttctcttt taaagttctt tatagggtta gggtgtggga 1440 aaatgctata ttaataaatc tgtagtgttt tgtgtttata tgttcagaac cagagtagac 1500 tggattgaaa gatggactgg gtctaattta tcatgactga tagatctggt taagttgtgt 1560 agtaaagcat taggagggtc attcytgtca caaaagtgcc actaaaacag cctcaggaga 1620 ataaatgact tgcttttcta aatctcaggt ttatctgggc tctatcatat agacaggctt 1680 ctgatagttt gcarctgtaa gcagaaacct acatatagtt aaaatcctgg tctttcttgg 1740 taaacagatt ttaaatgtct gatataaaac atgccacagg agaattcggg gatttgagtt 1800 tctctgaata gcatatatat gatgcatcgg ataggtcatt atgatttttt accatttcga 1860 cttacataat gaaaaccaat tcattttaaa tatcagatta ttattttgta agttgtggaa 1920 aaagctaatt gtagttttca ttatgaagtt ttcccaataa accaggtatt ctaaaaaaaa 1980 aaaaaaaa 1988 174 238 PRT Homo sapiens 174 Gly Ala Ala Ser Pro Arg Pro Leu Arg Phe Cys Gly Gly Ala Arg Ala 5 10 15 Arg Arg Pro Leu Ser Ala Val Ala Arg Pro Ala Arg Ser Ser Asp Pro 20 25 30 Leu Arg Ser Ala Pro Leu Gly Pro Ala Pro Pro Val Asn Met Ile Arg 35 40 45 Cys Gly Leu Ala Cys Glu Arg Cys Arg Trp Ile Leu Pro Leu Leu Leu 50 55 60 Leu Ser Ala Ile Ala Phe Asp Ile Ile Ala Leu Ala Gly Arg Gly Trp 65 70 75 80 Leu Gln Ser Ser Asp His Gly Gln Thr Ser Ser Leu Trp Trp Lys Cys 85 90 95 Ser Gln Glu Gly Gly Gly Ser Gly Ser Tyr Glu Glu Gly Cys Gln Ser 100 105 110 Leu Met Glu Tyr Ala Trp Gly Arg Ala Ala Ala Ala Met Leu Phe Cys 115 120 125 Gly Phe Ile Ile Leu Val Ile Cys Phe Ile Leu Ser Phe Phe Ala Leu 130 135 140 Cys Gly Pro Gln Met Leu Val Phe Leu Arg Val Ile Gly Gly Leu Leu 145 150 155 160 Ala Leu Ala Ala Val Phe Gln Ile Ile Ser Leu Val Ile Tyr Pro Val 165 170 175 Lys Tyr Thr Gln Thr Phe Thr Leu His Ala Asn Pro Ala Val Thr Tyr 180 185 190 Ile Tyr Asn Trp Ala Tyr Gly Phe Gly Trp Ala Ala Thr Ile Ile Leu 195 200 205 Ile Gly Cys Ala Phe Phe Phe Cys Cys Leu Pro Asn Tyr Glu Asp Asp 210 215 220 Leu Leu Gly Asn Ala Lys Pro Arg Tyr Phe Tyr Thr Ser Ala 225 230 235 175 4181 DNA Homo sapiens unsure (3347) n=A,T,C or G 175 ggtggatgcg tttgggttgt agctaggctt tttcttttct ttctctttta aaacacatct 60 agacaaggaa aaaacaagcc tcggatctga tttttcactc ctcgttcttg tgcttggttc 120 ttactgtgtt tgtgtatttt aaaggcgaga agacgagggg aacaaaacca gctggatcca 180 tccatcaccg tgggtggttt taatttttcg ttttttctcg ttattttttt ttaaacaacc 240 actcttcaca atgaacaaac tgtatatcgg aaacctcagc gagaacgccg ccccctcgga 300 cctagaaagt atcttcaagg acgccaagat cccggtgtcg ggacccttcc tggtgaagac 360 tggctacgcg ttcgtggact gcccggacga gagctgggcc ctcaaggcca tcgaggcgct 420 ttcaggtaaa atagaactgc acgggaaacc catagaagtt gagcactcgg tcccaaaaag 480 gcaaaggatt cggaaacttc agatacgaaa tatcccgcct catttacagt gggaggtgct 540 ggatagttta ctagtccagt atggagtggt ggagagctgt gagcaagtga acactgactc 600 ggaaactgca gttgtaaatg taacctattc cagtaaggac caagctagac aagcactaga 660 caaactgaat ggatttcagt tagagaattt caccttgaaa gtagcctata tccctgatga 720 aatggccgcc cagcaaaacc ccttgcagca gccccgaggt cgccgggggc ttgggcagag 780 gggctcctca aggcaggggt ctccaggatc cgtatccaag cagaaaccat gtgatttgcc 840 tctgcgcctg ctggttccca cccaatttgt tggagccatc ataggaaaag aaggtgccac 900 cattcggaac atcaccaaac agacccagtc taaaatcgat gtccaccgta aagaaaatgc 960 gggggctgct gagaagtcga ttactatcct ctctactcct gaaggcacct ctgcggcttg 1020 taagtctatt ctggagatta tgcataagga agctcaagat ataaaattca cagaagagat 1080 ccccttgaag attttagctc ataataactt tgttggacgt cttattggta aagaaggaag 1140 aaatcttaaa aaaattgagc aagacacaga cactaaaatc acgatatctc cattgcagga 1200 attgacgctg tataatccag aacgcactat tacagttaaa ggcaatgttg agacatgtgc 1260 caaagctgag gaggagatca tgaagaaaat cagggagtct tatgaaaatg atattgcttc 1320 tatgaatctt caagcacatt taattcctgg attaaatctg aacgccttgg gtctgttccc 1380 acccacttca gggatgccac ctcccacctc agggccccct tcagccatga ctcctcccta 1440 cccgcagttt gagcaatcag aaacggagac tgttcatcag tttatcccag ctctatcagt 1500 cggtgccatc atcggcaagc agggccagca catcaagcag ctttctcgct ttgctggagc 1560 ttcaattaag attgctccag cggaagcacc agatgctaaa gtgaggatgg tgattatcac 1620 tggaccacca gaggctcagt tcaaggctca gggaagaatt tatggaaaaa ttaaagaaga 1680 aaactttgtt agtcctaaag aagaggtgaa acttgaagct catatcagag tgccatcctt 1740 tgctgctggc agagttattg gaaaaggagg caaaacggtg aatgaacttc agaatttgtc 1800 aagtgcagaa gttgttgtcc ctcgtgacca gacacctgat gagaatgacc aagtggttgt 1860 caaaataact ggtcacttct atgcttgcca ggttgcccag agaaaaattc aggaaattct 1920 gactcaggta aagcagcacc aacaacagaa ggctctgcaa agtggaccac ctcagtcaag 1980 acggaagtaa aggctcagga aacagcccac cacagaggca gatgccaaac caaagacaga 2040 ttgcttaacc aacagatggg cgctgacccc ctatccagaa tcacatgcac aagtttttac 2100 ctagccagtt gtttctgagg accaggcaac ttttgaactc ctgtctctgt gagaatgtat 2160 actttatgct ctctgaaatg tatgacaccc agctttaaaa caaacaaaca aacaaacaaa 2220 aaaagggtgg gggagggagg gaaagagaag agctctgcac ttccctttgt tgtagtctca 2280 cagtataaca gatattctaa ttcttcttaa tattccccca taatgccaga aattggctta 2340 atgatgcttt cactaaattc atcaaataga ttgctcctaa atccaattgt taaaattgga 2400 tcagaataat tatcacagga acttaaatgt taagccatta gcatagaaaa actgttctca 2460 gttttatttt tacctaacac taacatgagt aacctaaggg aagtgctgaa tggtgttggc 2520 aggggtatta aacgtgcatt tttactcaac tacctcaggt attcagtaat acaatgaaaa 2580 gcaaaattgt tccttttttt tgaaaatttt atatacttta taatgataga agtccaaccg 2640 ttttttaaaa aataaattta aaatttaaca gcaatcagct aacaggcaaa ttaagatttt 2700 tacttctggc tggtgacagt aaagctggaa aattaatttc agggtttttt gaggcttttg 2760 acacagttat tagttaaatc aaatgttcaa aaatacggag cagtgcctag tatctggaga 2820 gcagcactac catttattct ttcatttata gttgggaaag tttttgacgg tactaacaaa 2880 gtggtcgcag gagattttgg aacggctggt ttaaatggct tcaggagact tcagtttttt 2940 gtttagctac atgattgaat gcataataaa tgctttgtgc ttctgactat caatacctaa 3000 agaaagtgca tcagtgaaga gatgcaagac tttcaactga ctggcaaaaa gcaagcttta 3060 gcttgtctta taggatgctt agtttgccac tacacttcag accaatggga cagtcataga 3120 tggtgtgaca gtgtttaaac gcaacaaaag gctacatttc catggggcca gcactgtcat 3180 gagcctcact aagctatttt gaagattttt aagcactgat aaattaaaaa aaaaaaaaaa 3240 aaattagact ccaccttaag tagtaaagta taacaggatt tctgtatact gtgcaatcag 3300 ttctttgaaa aaaaagtcaa aagatagaga atacaagaaa agttttnggg atataatttg 3360 aatgactgtg aaaacatatg acctttgata acgaactcat ttgctcactc cttgacagca 3420 aagcccagta cgtacaattg tgttgggtgt gggtggtctc caaggccacg ctgctctctg 3480 aattgatttt ttgagttttg gnttgnaaga tgatcacagn catgttacac tgatcttnaa 3540 ggacatatnt tataaccctt taaaaaaaaa atcccctgcc tcattcttat ttcgagatga 3600 atttcgatac agactagatg tctttctgaa gatcaattag acattntgaa aatgatttaa 3660 agtgttttcc ttaatgttct ctgaaaacaa gtttcttttg tagttttaac caaaaaagtg 3720 ccctttttgt cactggtttc tcctagcatt catgattttt ttttcacaca atgaattaaa 3780 attgctaaaa tcatggactg gctttctggt tggatttcag gtaagatgtg tttaaggcca 3840 gagcttttct cagtatttga tttttttccc caatatttga ttttttaaaa atatacacat 3900 aggagctgca tttaaaacct gctggtttaa attctgtcan atttcacttc tagcctttta 3960 gtatggcnaa tcanaattta cttttactta agcatttgta atttggagta tctggtacta 4020 gctaagaaat aattcnataa ttgagttttg tactcnccaa anatgggtca ttcctcatgn 4080 ataatgtncc cccaatgcag cttcattttc caganacctt gacgcaggat aaattttttc 4140 atcatttagg tccccaaaaa aaaaaaaaaa aaaaaaaaaa a 4181 176 579 PRT Homo sapiens 176 Met Asn Lys Leu Tyr Ile Gly Asn Leu Ser Glu Asn Ala Ala Pro Ser 5 10 15 Asp Leu Glu Ser Ile Phe Lys Asp Ala Lys Ile Pro Val Ser Gly Pro 20 25 30 Phe Leu Val Lys Thr Gly Tyr Ala Phe Val Asp Cys Pro Asp Glu Ser 35 40 45 Trp Ala Leu Lys Ala Ile Glu Ala Leu Ser Gly Lys Ile Glu Leu His 50 55 60 Gly Lys Pro Ile Glu Val Glu His Ser Val Pro Lys Arg Gln Arg Ile 65 70 75 80 Arg Lys Leu Gln Ile Arg Asn Ile Pro Pro His Leu Gln Trp Glu Val 85 90 95 Leu Asp Ser Leu Leu Val Gln Tyr Gly Val Val Glu Ser Cys Glu Gln 100 105 110 Val Asn Thr Asp Ser Glu Thr Ala Val Val Asn Val Thr Tyr Ser Ser 115 120 125 Lys Asp Gln Ala Arg Gln Ala Leu Asp Lys Leu Asn Gly Phe Gln Leu 130 135 140 Glu Asn Phe Thr Leu Lys Val Ala Tyr Ile Pro Asp Glu Met Ala Ala 145 150 155 160 Gln Gln Asn Pro Leu Gln Gln Pro Arg Gly Arg Arg Gly Leu Gly Gln 165 170 175 Arg Gly Ser Ser Arg Gln Gly Ser Pro Gly Ser Val Ser Lys Gln Lys 180 185 190 Pro Cys Asp Leu Pro Leu Arg Leu Leu Val Pro Thr Gln Phe Val Gly 195 200 205 Ala Ile Ile Gly Lys Glu Gly Ala Thr Ile Arg Asn Ile Thr Lys Gln 210 215 220 Thr Gln Ser Lys Ile Asp Val His Arg Lys Glu Asn Ala Gly Ala Ala 225 230 235 240 Glu Lys Ser Ile Thr Ile Leu Ser Thr Pro Glu Gly Thr Ser Ala Ala 245 250 255 Cys Lys Ser Ile Leu Glu Ile Met His Lys Glu Ala Gln Asp Ile Lys 260 265 270 Phe Thr Glu Glu Ile Pro Leu Lys Ile Leu Ala His Asn Asn Phe Val 275 280 285 Gly Arg Leu Ile Gly Lys Glu Gly Arg Asn Leu Lys Lys Ile Glu Gln 290 295 300 Asp Thr Asp Thr Lys Ile Thr Ile Ser Pro Leu Gln Glu Leu Thr Leu 305 310 315 320 Tyr Asn Pro Glu Arg Thr Ile Thr Val Lys Gly Asn Val Glu Thr Cys 325 330 335 Ala Lys Ala Glu Glu Glu Ile Met Lys Lys Ile Arg Glu Ser Tyr Glu 340 345 350 Asn Asp Ile Ala Ser Met Asn Leu Gln Ala His Leu Ile Pro Gly Leu 355 360 365 Asn Leu Asn Ala Leu Gly Leu Phe Pro Pro Thr Ser Gly Met Pro Pro 370 375 380 Pro Thr Ser Gly Pro Pro Ser Ala Met Thr Pro Pro Tyr Pro Gln Phe 385 390 395 400 Glu Gln Ser Glu Thr Glu Thr Val His Gln Phe Ile Pro Ala Leu Ser 405 410 415 Val Gly Ala Ile Ile Gly Lys Gln Gly Gln His Ile Lys Gln Leu Ser 420 425 430 Arg Phe Ala Gly Ala Ser Ile Lys Ile Ala Pro Ala Glu Ala Pro Asp 435 440 445 Ala Lys Val Arg Met Val Ile Ile Thr Gly Pro Pro Glu Ala Gln Phe 450 455 460 Lys Ala Gln Gly Arg Ile Tyr Gly Lys Ile Lys Glu Glu Asn Phe Val 465 470 475 480 Ser Pro Lys Glu Glu Val Lys Leu Glu Ala His Ile Arg Val Pro Ser 485 490 495 Phe Ala Ala Gly Arg Val Ile Gly Lys Gly Gly Lys Thr Val Asn Glu 500 505 510 Leu Gln Asn Leu Ser Ser Ala Glu Val Val Val Pro Arg Asp Gln Thr 515 520 525 Pro Asp Glu Asn Asp Gln Val Val Val Lys Ile Thr Gly His Phe Tyr 530 535 540 Ala Cys Gln Val Ala Gln Arg Lys Ile Gln Glu Ile Leu Thr Gln Val 545 550 555 560 Lys Gln His Gln Gln Gln Lys Ala Leu Gln Ser Gly Pro Pro Gln Ser 565 570 575 Arg Arg Lys 177 401 DNA Homo sapiens 177 atgccccgta aatgtcttca gtgttcttca gggtagttgg gatctcaaaa gatttggttc 60 agatccaaac aaatacacat tctgtgtttt agctcagtgt tttctaaaaa aagaaactgc 120 cacacagcaa aaaattgttt actttgttgg acaaaccaaa tcagttctca aaaaatgacc 180 ggtgcttata aaaagttata aatatcgagt agctctaaaa caaaccacct gaccaagagg 240 gaagtgagct tgtgcttagt atttacattg gatgccagtt ttgtaatcac tgacttatgt 300 gcaaactggt gcagaaattc tataaactct ttgctgtttt tgatacctgc tttttgtttc 360 attttgtttt gttttgtaaa aatgataaaa cttcagaaaa t 401 178 561 DNA Homo sapiens 178 acgcctttca agggtgtacg caaagcactc attgataccc ttttggatgg ctatgaaaca 60 gcccgctatg ggacaggggt ctttggccag aatgagtacc tacgctatca ggaggccctg 120 agtgagctgg ccactgcggt taaagcacga attgggagct ctcagcgaca tcaccagtca 180 gcagccaaag acctaactca gtcccctgag gtctccccaa caaccatcca ggtgacatac 240 ctcccctcca gtcagaagag taaacgtgcc aagcacttcc ttgaattgaa gagctttaag 300 gataactata acacattgga gagtactctg tgacggagct gaaggactct tgccgtagat 360 taagccagtc agttgcaatg tgcaagacag gctgcttgcc gggccgccct cggaacatct 420 ggcccagcag gcccagactg tatccatcca agttcccgtt gtatccagag ttcttagagc 480 ttgtgtctaa agggtaattc cccaaccctt ccttatgagc atttttagaa cattggctaa 540 gactattttc ccccagtagc g 561 179 521 DNA Homo sapiens 179 cccaacgcgt ttgcaaatat tcccctggta gcctacttcc ttacccccga atattggtaa 60 gatcgagcaa tggcttcagg acatgggttc tcttctcctg tgatcattca agtgctcact 120 gcatgaagac tggcttgtct cagtgtttca acctcaccag ggctgtctct tggtccacac 180 ctcgctccct gttagtgccg tatgacagcc cccatcaaat gaccttggcc aagtcacggt 240 ttctctgtgg tcaaggttgg ttggctgatt ggtggaaagt agggtggacc aaaggaggcc 300 acgtgagcag tcagcaccag ttctgcacca gcagcgcctc cgtcctagtg ggtgttcctg 360 tttctcctgg ccctgggtgg gctagggcct gattcgggaa gatgcctttg cagggagggg 420 aggataagtg ggatctacca attgattctg gcaaaacaat ttctaagatt tttttgcttt 480 atgtgggaaa cagatctaaa tctcatttta tgctgtattt t 521 180 417 DNA Homo sapiens 180 ggtggaattc gccgaagatg gcggaggtgc aggtcctggt gcttgatggt cgaggccatc 60 tcctgggccg cctggcggcc atcgtggcta aacaggtact gctgggccgg aaggtggtgg 120 tcgtacgctg tgaaggcatc aacatttctg gcaatttcta cagaaacaag ttgaagtacc 180 tggctttcct ccgcaagcgg atgaacacca acccttcccg aggcccctac cacttccggg 240 cccccagccg catcttctgg cggaccgtgc gaggtatgct gccccacaaa accaagcgag 300 gccaggccgc tctggaccgt ctcaaggtgt ttgacggcat cccaccgccc tacgacaaga 360 aaaagcggat ggtggttcct gctgccctca aggtcgtgcg tctgaagcct acaagaa 417 181 283 DNA Homo sapiens unsure (35) n=A,T,C or G 181 gatttcttct aaataggatg taaaacttct ttcanattac tcttcctcag tcctgcctgc 60 caagaactca agtgtaactg tgataaaata acctttccca ggtatattgg caggtatgtg 120 tgtaatctca gaatacacag gtgacataga tatgatatga caactggtaa tggtggattc 180 atttacattg tttacacttc tatgaccagg ccttaaggga aggtcagttt tttaaaaaac 240 caagtagtgt cttcctacct atctccagat acatgtcaaa aaa 283 182 401 DNA Homo sapiens 182 atattcttgc tgcttatgca gctgacattg ttgccctccc taaagcaacc aagtagcctt 60 tatttcccac agtgaaagaa aacgctggcc tatcagttac attacaaaag gcagatttca 120 agaggattga gtaagtagtt ggatggcttt cataaaaaca agaattcaag aagaggattc 180 atgctttaag aaacatttgt tatacattcc tcacaaatta tacctgggat aaaaactatg 240 tagcaggcag tgtgttttcc ttccatgtct ctctgcacta cctgcagtgt gtcctctgag 300 gctgcaagtc tgtcctatct gaattcccag cagaagcact aagaagctcc accctatcac 360 ctagcagata aaactatggg gaaaacttaa atctgtgcat a 401 183 366 DNA Homo sapiens unsure (325) n=A,T,C or G 183 accgtgtcca agtttttaga acccttgtta gccagaccga ggtgtcctgg tcaccgtttc 60 accatcatgc tttgatgttc ccctgtcttt ctctcttctg ctctcaagag caaaggttaa 120 tttaaggaca aagatgaagt cactgtaaac taatctgtca ttgtttttac cttccttttc 180 tttttcagtg cagaaattaa aagtaagtat aaagcaccgt gattgggagt gtttttgcgt 240 gtgtcggaat cactggtaaa tgttggctga gaacaatccc tccccttgca cttgtgaaaa 300 cactttgagc gctttaagag attancctga gaaataatta aatatctttt ctcttcaaaa 360 aaaaaa 366 184 370 DNA Homo sapiens 184 tcttacttca aaagaaaaat aaacataaaa aataagttgc tggttcctaa caggaaaaat 60 tttaataatt gtactgagag aaactgctta cgtacacatt gcagatcaaa tatttggagt 120 taaaatgtta gtctacatag atgggtgatt gtaactttat tgccattaaa agatttcaaa 180 ttgcattcat gcttctgtgt acacataatg aaaaatgggc aaataatgaa gatctctcct 240 tcagtctgct ctgtttaatt ctgctgtctg ctcttctcta atgctgcgtc cctaattgta 300 cacagtttag tgatatctag gagtataaag ttgtcgccca tcaataaaaa tcacaaagtt 360 ggtttaaaaa 370 185 107 DNA Homo sapiens 185 ctcatattat tttccttttg agaaattgga aactctttct gttgctatta tattaataaa 60 gttggtgttt attttctggt agtcaccttc cccatttaaa aaaaaaa 107 186 309 DNA Homo sapiens 186 gaaaggatgg ctctggttgc cacagagctg ggacttcatg ttcttctaga gagggccaca 60 agagggccac aggggtggcc gggagttgtc agctgatgcc tgctgagagg caggaattgt 120 gccagtgagt gacagtcatg agggagtgtc tcttcttggg gaggaaagaa ggtagagcct 180 ttctgtctga atgaaaggcc aaggctacag tacagggccc cgccccagcc agggtgttaa 240 tgcccacgta gtggaggcct ctggcagatc ctgcattcca aggtcactgg actgtacgtt 300 tttatggtt 309 187 477 DNA Homo sapiens 187 ttcagtccta gcaagaagcg agaattctga gatcctccag aaagtcgagc agcacccacc 60 tccaacctcg ggccagtgtc ttcaggcttt actggggacc tgcgagctgg cctaatgtgg 120 tggcctgcaa gccaggccat ccctgggcgc cacagacgag ctccgagcca ggtcaggctt 180 cggaggccac aagctcagcc tcaggcccag gcactgattg tggcagaggg gccactaccc 240 aaggtctagc taggcccaag acctagttac ccagacagtg agaagcccct ggaaggcaga 300 aaagttggga gcatggcaga cagggaaggg aaacattttc agggaaaaga catgtatcac 360 atgtcttcag aagcaagtca ggtttcatgt aaccgagtgt cctcttgcgt gtccaaaagt 420 agcccagggc tgtagcacag gcttcacagt gattttgtgt tcagccgtga gtcacac 477 188 220 DNA Homo sapiens 188 taaatatggt agatattaat attcctctta gatgaccagt gattccaatt gtcccaagtt 60 ttaaataagt accctgtgag tatgagataa attagtgaca atcagaacaa gtttcagtat 120 cagatgttca agaggaagtt gctattgcat tgattttaat atttgtacat aaacactgat 180 ttttttgagc attattttgt atttgttgta ctttaatacc 220 189 417 DNA Homo sapiens unsure (76) n=A,T,C or G 189 accatcttga cagaggatac atgctcccaa aacgtttgtt accacactta aaaatcactg 60 ccatcattaa gcatcnnttt caaaattata gccattcatg atttactttt tccagatgac 120 tatcattatt ctagtccttt gaatttgtaa ggggaaaaaa aacaaaaaca aaaacttacg 180 atgcactttt ctccagcaca tcagatttca aattgaaaat taaagacatg ctatggtaat 240 gcacttgcta gtactacaca ctttgtacaa caaaaaacag aggcaagaaa caacggaaag 300 agaaaagcct tcctttgttg gcccttaaac tgagtcaaga tctgaaatgt agagatgatc 360 tctgacgata cctgtatgtt cttattgtgt aaataaaatt gctggtatga aatgaca 417 190 497 DNA Homo sapiens 190 gcactgcggc gctctcccgt cccgcggtgg ttgctgctgc tgccgctgct gctgggcctg 60 aacgcaggag ctgtcattga ctggcccaca gaggagggca aggaagtatg ggattatgtg 120 acggtccgca aggatgccta catgttctgg tggctctatt atgccaccaa ctcctgcaag 180 aacttctcag aactgcccct ggtcatgtgg cttcagggcg gtccaggcgg ttctagcact 240 ggatttggaa actttgagga aattgggccc cttgacagtg atctcaaacc acggaaaacc 300 acctggctcc aggctgccag tctcctattt gtggataatc ccgtgggcac tgggttcagt 360 tatgtgaatg gtagtggtgc ctatgccaag gacctggcta tggtggcttc agacatgatg 420 gttctcctga agaccttctt cagttgccac aaagaattcc agacagttcc attctacatt 480 ttctcagagt cctatgg 497 191 175 DNA Homo sapiens 191 atgttgaata ttttgcttat taactttgtt tattgtcttc tccctcgatt agaatattag 60 ctacttgagt acaaggattt gagcctgtta cattcactgc tgaattttag gctcctggaa 120 gatacccagc attcaataga gaccacacaa taaatatatg tcaaataaaa aaaaa 175 192 526 DNA Homo sapiens 192 agtaaacatt attatttttt ttatatttgc aaaggaaaca tatctaatcc ttcctataga 60 aagaacagta ttgctgtaat tccttttctt ttcttcctca tttcctctgc cccttaaaag 120 attgaagaaa gagaaacttg tcaactcata tccacgttat ctagcaaagt acataagaat 180 ctatcactaa gtaatgtatc cttcagaatg tgttggttta ccagtgacac cccatattca 240 tcacaaaatt aaagcaagaa gtccatagta atttatttgc taatagtgga tttttaatgc 300 tcagagtttc tgaggtcaaa ttttatcttt tcacttacaa gctctatgat cttaaataat 360 ttacttaatg tattttggtg tattttcctc aaattaatat tggtgttcaa gactatatct 420 aattcctctg atcactttga gaaacaaact tttattaaat gtaaggcact tttctatgaa 480 ttttaaatat aaaaataaat attgttctga ttattactga aaaaaa 526 193 553 DNA Homo sapiens unsure (290) n=A,T,C or G 193 tccattgtgg tggaattcgc tctctggtaa aggcgtgcag gtgttggccg cggcctctga 60 gctgggatga gccgtgctcc cggtggaagc aagggagccc agccggagcc atggccagta 120 cagtggtagc agttggactg accattgctg ctgcaggatt tgcaggccgt tacgttttgc 180 aagccatgaa gcatatggag cctcaagtaa aacaagtttt tcaaagccta ccaaaatctg 240 ccttcagtgg tggctattat agaggtgggt ttgaacccaa aatgacaaan cgggaagcan 300 cattaatact aggtgtaagc cctactgcca ataaagggaa aataagagat gctcatcgac 360 gaattatgct tttaaatcat cctgacaaag gaggatctcc ttatatagca nccaaaatca 420 atgaagctaa agatttacta naaggtcaag ctaaaaaatg aagtaaatgt atgatgaatt 480 ttaagttcgt attagtttat gtatatgagt actaagtttt tataataaaa tgcctcagag 540 ctacaatttt aaa 553 194 320 DNA Homo sapiens 194 cccttcccaa tccatcagta aagaccccat ctgccttgtc catgccgttt cccaacaggg 60 atgtcacttg atatgagaat ctcaaatctc aatgccttat aagcattcct tcctgtgtcc 120 attaagactc tgataattgt ctcccctcca taggaatttc tcccaggaaa gaaatatatc 180 cccatctccg tttcatatca gaactaccgt ccccgatatt cccttcagag agattaaaga 240 ccagaaaaaa gtgagcctct tcatctgcac ctgtaatagt ttcagttcct attttcttcc 300 attgacccat atttatacct 320 195 320 DNA Homo sapiens unsure (203) n=A,T,C or G 195 aagcatgacc tggggaaatg gtcagacctt gtattgtgtt tttggccttg aaagtagcaa 60 gtgaccagaa tctgccatgg caacaggctt taaaaaagac ccttaaaaag acactgtctc 120 aactgtggtg ttagcaccag ccagctctct gtacatttgc tagcttgtag ttttctaaga 180 ctgagtaaac ttcttatttt tanaaagggg aggctggntt gtaactttcc ttgtacttaa 240 ttgggtaaaa gtcttttcca caaaccacca tctattttgt gaactttgtt agtcatcttt 300 tatttggtaa attatgaact 320 196 357 DNA Homo sapiens unsure (36) n=A,T,C or G 196 atataaaata atacgaaact ttaaaaagca ttggantgtc agtatgttga atcagtagtt 60 tcactttaac tgtaaacaat ttcttaggac accatttggg ctagtttctg tgtaagtgta 120 aatactacaa aaacttattt atactgttct tatgtcattt gttatattca tagatttata 180 tgatgatatg acatctggct aaaaagaaat tattgcaaaa ctaaccacta tgtacttttt 240 tataaatact gtatggacaa aaaatggcat tttttatatt aaattgttta gctctggcaa 300 aaaaaaaaaa ttttaagagc tggtactaat aaaggattat tatgactgtt aaaaaaa 357 197 565 DNA Homo sapiens unsure (27) n=A,T,C or G 197 tcagctgagt accatcagga tatttanccc tttaagtgct gttttgggag tagaaaacta 60 aagcaacaat acttcctctt gacagctttg attggaatgg ggttattaga tcattcacct 120 tggtcctaca ctttttagga tgcttggtga acataacacc acttataatg aacatccctg 180 gttcctatat tttgggctat gtgggtagga attgttactt gttactgcag cagcagccct 240 agaaagtaag cccagggctt cagatctaag ttagtccaaa agctaaatga tttaaagtca 300 agttgtaatg ctaggcataa gcactctata atacattaaa ttataggccg agcaattagg 360 gaatgtttct gaaacattaa acttgtattt atgtcactaa aattctaaca caaacttaaa 420 aaatgtgtct catacatatg ctgtactagg cttcatcatg catttctaaa tttgtgtatg 480 atttgaatat atgaaagaat ttatacaaga gtgttattta aaattattaa aaataaatgt 540 atataatttg tacctattgt aaaaa 565 198 484 DNA Homo sapiens 198 tatgtaagta ttggtgtctg ctttaaaaaa ggagacccag acttcacctg tcctttttaa 60 acatttgaga acagtgttac tctgagcagt tgggccacct tcaccttatc cgacagctga 120 ctgttggatg tgtccattgt cgccagtttg gctgttgccc ggacaggaca ggacctccat 180 tgggcgcagc agcaggtggc aggggtgtgg cttgaggtgg gtggcagcgt ctggtcctcc 240 tctctggtgc tttctgagag ggtctctaaa gcagagtgtg gttggcctgg gggaaggcag 300 agcacgtatt tctcccctct agtacctctg catttgtgag tgttccctct ggctttctga 360 agggcagcag actcttgagt atactgcaga ggacatgctt tatcagtagg tcctgagggc 420 tccaggggct caactgacca agtaacacag aagttggggt atgtggccta tttgggtcgg 480 aaac 484 199 429 DNA Homo sapiens unsure (77) n=A,T,C or G 199 gcttatgttt tttgttttaa cttttgtttt ttaacattta gaatattaca ttttgtatta 60 tacagtacct ttctcanaca ttttgtanaa ttcatttcgg cagctcacta ggattttgct 120 gaacattaaa aagngtgata gcgatattag ngccaatcaa atggaaaaaa ggtagtctta 180 ataaacaana cacaacgttt ttatacaaca tactttaaaa tattaanaaa actccttaat 240 attgtttcct attaagtatt attctttggg caanattttc tgatgctttt gattttctct 300 caatttagca tttgctttng gtttttttct ctatttagca ttctgttaag gcacaaaaac 360 tatgtactgt atgggaaatg ttgtaaatat taccttttcc acattttaaa cagacaactt 420 tgaatccaa 429 200 279 DNA Homo sapiens 200 gcttttttga ggaattacag ggaagctcct ggaattgtac atggatatct ttatccctag 60 ggggaaatca aggagctggg cacccctaat tctttatgga agtgtttaaa actattttaa 120 ttttattaca agtattacta gagtagtggt tctactctaa gatttcaaaa gtgcatttaa 180 aatcatacat gttcccgcct gcaaatatat tgttattttg gtggagaaaa aaatagtata 240 ttctacataa aaaattaaag atattaacta agaaaaaaa 279 201 569 DNA Homo sapiens 201 taggtcagta tttttagaaa ctcttaatag ctcatactct tgataccaaa agcagccctg 60 attgttaaag cacacacctg cacaagaagc agtgatggtt gcatttacat ttcctgggtg 120 cacaaaaaaa aattctcaaa aagcaaggac ttacgctttt tgcaaagcct ttgagaagtt 180 actggatcat aggaagctta taacaagaat ggaagattct taaataactc actttctttg 240 gtatccagta acagtagatg ttcaaaatat gtagctgatt aataccagca ttgtgaacgc 300 tgtacaacct tgtggttatt actaagcaag ttactactag cttctgaaaa gtagcttcat 360 aattaatgtt atttatacac tgccttccat gacttttact ttgccctaag ctaatctcca 420 aaatctgaaa tgctactcca atatcagaaa aaaaggggga ggtggaatta tatttcctgt 480 gattttaaga gtacagagaa tcatgcacat ctctgattag ttcatatatg tctagtgtgt 540 aataaaagtc aaagatgaac tctcaaaaa 569 202 501 DNA Homo sapiens 202 attaataggc ttaataattg ttggcaagga tccttttgct ttctttggca tgcaagctcc 60 tagcatctgg cagtggggcc aagaaaataa ggtttatgca tgtatgatgg ttttcttctt 120 gagcaacatg attgagaacc agtgtatgtc aacaggtgca tttgagataa ctttaaatga 180 tgtacctgtg tggtctaagc tggaatctgg tcaccttcca tccatgcaac aacttgttca 240 aattcttgac aatgaaatga agctcaatgt gcatatggat tcaatcccac accatcgatc 300 atagcaccac ctatcagcac tgaaaactct tttgcattaa gggatcattg caagagcagc 360 gtgactgaca ttatgaaggc ctgtactgaa gacagcaagc tgttagtaca gaccagatgc 420 tttcttggca ggctcgttgt acctcttgga aaacctcaat gcaagatagt gtttcagtgc 480 tggcatattt tggaattctg c 501 203 261 DNA Homo sapiens unsure (36) n=A,T,C or G 203 gacaagctcc tggtcttgag atgtcttctc gttaangaga tgggcctttt ggaggtaaag 60 gataaaatga atgagttctg tcatgattca ctattntata acttgcatga cctttactgt 120 gttagctctt tgaatgttct tgaaatttta gactttcttt gtaaacaaat gatatgtcct 180 tatcattgta taaaagctgt tatgtgcaac agtgtggaga ttccttgtct gatttaataa 240 aatacttaaa cactgaaaaa a 261 204 421 DNA Homo sapiens 204 agcatctttt ctacaacgtt aaaattgcag aagtagctta tcattaaaaa acaacaacaa 60 caacaataac aataaatcct aagtgtaaat cagttattct accccctacc aaggatatca 120 gcctgttttt tccctttttt ctcctgggaa taattgtggg cttcttccca aatttctaca 180 gcctctttcc tcttctcatg cttgagcttc cctgtttgca cgcatgcgtg tgcaggactg 240 gcttgtgtgc ttggactcgg ctccaggtgg aagcatgctt tcccttgtta ctgttggaga 300 aactcaaacc ttcaagccct aggtgtagcc attttgtcaa gtcatcaact gtatttttgt 360 actggcatta acaaaaaaag aagataaaat attgtaccat taaactttaa taaaacttta 420 a 421 205 460 DNA Homo sapiens 205 tactctcaca atgaaggacc tggaatgaaa aatctgtgtc taaacaagtc ctctttagat 60 tttagtgcaa atccagagcc agcgtcggtt gcctcgagta attctttcat gggtaccttt 120 ggaaaagctc tcaggagacc tcacctagat gcctattcaa gctttggaca gccatcagat 180 tgtcagccaa gagcctttta tttgaaagct cattcttccc cagacttgga ctctgggtca 240 gaggaagatg ggaaagaaag gacagatttt caggaagaaa atcacatttg tacctttaaa 300 cagactttag aaaactacag gactccaaat tttcagtctt atgacttgga cacatagact 360 gaatgagacc aaaggaaaag cttaacatac tacctcaagg tgaactttta tttaaaagag 420 agagaatctt atgtttttta aatggagtta tgaattttaa 460 206 481 DNA Homo sapiens 206 tgtggtggaa ttcgggacgc ccccagaccc tgactttttc ctgcgtgggc cgtctcctcc 60 tgcggaagca gtgacctctg acccctggtg accttcgctt tgagtgcctt ttgaacgctg 120 gtcccgcggg acttggtttt ctcaagctct gtctgtccaa agacgctccg gtcgaggtcc 180 cgcctgccct gggtggatac ttgaacccca gacgcccctc tgtgctgctg tgtccggagg 240 cggccttccc atctgcctgc ccacccggag ctctttccgc cggcgcaggg tcccaagccc 300 acctcccgcc ctcagtcctg cggtgtgcgt ctgggcacgt cctgcacaca caatgcaagt 360 cctggcctcc gcgcccgccc gcccacgcga gccgtacccg ccgccaactc tgttatttat 420 ggtgtgaccc cctggaggtg ccctcggccc accggggcta tttattgttt aatttatttg 480 t 481 207 605 DNA Homo sapiens 207 accctttttg gattcagggc tcctcacaat taaaatgagt gtaatgaaac aaggtgaaaa 60 tatagaagca tccctttgta tactgttttg ctacttacag tgtacttggc attgctttat 120 ctcactggat tctcacggta ggatttctga gatcttaatc taagctccaa agttgtctac 180 ttttttgatc ctagggtgct ccttttgttt tacagagcag ggtcacttga tttgctagct 240 ggtggcagaa ttggcaccat tacccaggtc tgactgacca ccagtcagag gcactttatt 300 tgtatcatga aatgatttga aatcattgta aagcagcgaa gtctgataat gaatgccagc 360 tttccttgtg ctttgataac aaagactcca aatattctgg agaacctgga taaaagtttg 420 aagggctaga ttgggatttg aagacaaaat tgtaggaaat cttacatttt tgcaataaca 480 aacattaatg aaagcaaaac attataaaag taattttaat tcaccacata cttatcaatt 540 tcttgatgct tccaaatgac atctaccaga tatggttttg tggacatctt tttctgttta 600 cataa 605 208 655 DNA Homo sapiens 208 ggcgttgttc tggattcccg tcgtaactta aagggaaact ttcacaatgt ccggagccct 60 tgatgtcctg caaatgaagg aggaggatgt ccttaagttc cttgcagcag gaacccactt 120 aggtggcacc aatcttgact tccagatgga acagtacatc tataaaagga aaagtgatgg 180 catctatatc ataaatctca agaggacctg ggagaagctt ctgctggcag ctcgtgcaat 240 tgttgccatt gaaaaccctg ctgatgtcag tgttatatcc tccaggaata ctggccagag 300 ggctgtgctg aagtttgctg ctgccactgg agccactcca attgctggcc gcttcactcc 360 tggaaccttc actaaccaga tccaggcagc cttccgggag ccacggcttc ttgtggttac 420 tgaccccagg gctgaccacc agcctctcac ggaggcatct tatgttaacc tacctaccat 480 tgcgctgtgt aacacagatt ctcctctgcg ctatgtggac attgccatcc catgcaacaa 540 caagggagct cactcagtgg gtttgatgtg gtggatgctg gctcgggaag ttctgcgcat 600 gcgtggcacc atttcccgtg aacacccatg ggaggtcatg cctgatctgt acttc 655 209 621 DNA Homo sapiens 209 catttagaac atggttatca tccaagacta ctctaccctg caacattgaa ctcccaagag 60 caaatccaca ttcctcttga gttctgcagc ttctgtgtaa atagggcagc tgtcgtctat 120 gccgtagaat cacatgatct gaggaccatt catggaagct gctaaatagc ctagtctggg 180 gagtcttcca taaagttttg catggagcaa acaaacagga ttaaactagg tttggttcct 240 tcagccctct aaaagcatag ggcttagcct gcaggcttcc ttgggctttc tctgtgtgtg 300 tagttttgta aacactatag catctgttaa gatccagtgt ccatggaaac cttcccacat 360 gccgtgactc tggactatat cagtttttgg aaagcagggt tcctctgcct gctaacaagc 420 ccacgtggac cagtctgaat gtctttcctt tacacctatg tttttaaata gtcaaacttc 480 aagaaacaat ctaaacaagt ttctgttgca tatgtgtttg tgaacttgta tttgtattta 540 gtaggcttct atattgcatt taacttgttt ttgtaactcc tgattcttcc ttttcggata 600 ctattgatga ataaagaaat t 621 210 533 DNA Homo sapiens unsure (20) n=A,T,C or G 210 cgccttgggg agccggcggn ngagtccggg acgtggagac ccggggtccc ggcagccggg 60 nggcccgcgg gcccagggtg gggatgcacc gccgcggggt gggagctggc gccatcgcca 120 agaagaaact tgcagaggcc aagtataagg agcgagggac ggtcttggct gaggaccagc 180 tagcccagat gtcaaagcag ttggacatgt tcaagaccaa cctggaggaa tttgccagca 240 aacacaagca ggagatccgg aagaatcctg agttccgtgt gcagttccag gacatgtgtg 300 caaccattgg cgtggatccg ctggcctctg gaaaaggatt ttggtctgag atgctgggcg 360 tgggggactt ctattacgaa ctaggtgtcc aaattatcga agtgtgcctg gcgctgaagc 420 atcggaatgg aggtctgata actttggagg aactacatca acaggtgttg aagggaaggg 480 gcaagttcgc ccaggatgtc agtcaagatg acctgatcag agccatcaag aaa 533 211 451 DNA Homo sapiens 211 ttagcttgag ccgagaacga ggcgagaaag ctggagaccg aggagaccgc ctagagcgga 60 gtgaacgggg aggggaccgt ggggaccggc ttgatcgtgc gcggacacct gctaccaagc 120 ggagcttcag caaggaagtg gaggagcgga gtagagaacg gccctcccag cctgaggggc 180 tgcgcaaggc agctagcctc acggaggatc gggaccgtgg gcgggatgcc gtgaagcgag 240 aagctgccct acccccagtg agccccctga aggcggctct ctctgaggag gagttagaga 300 agaaatccaa ggctatcatt gaggaatatc tccatctcaa tgacatgaaa gaggcagtcc 360 agtgcgtgca ggagctggcc tcaccctcct tgctcttcat ctttgtacgg catggtgtcg 420 agtctacgct ggagcgcagt gccattgctc g 451 212 471 DNA Homo sapiens unsure (54) n=A,T,C or G 212 gtgattattc ttgatcaggg agaagatcat ttagatttgt tttgcattcc ttanaatgga 60 gggcaacatt ccacagctgc cctggctgtg atgagtgtcc ttgcaggggc cggagtagga 120 gcactggggt gggggcggaa ttggggttac tcgatgtaag ggattccttg ttgttgtgtt 180 gagatccagt gcagttgtga tttctgtgga tcccagcttg gttccaggaa ttttgtgtga 240 ttggcttaaa tccagttttc aatcttcgac agctgggctg gaacgtgaac tcagtagctg 300 aacctgtctg acccggtcac gttcttggat cctcagaact ctttgctctt gtcggggtgg 360 gggtgggaac tcacgtgggg agcggtggct gagaaaatgt aaggattctg gaatacatat 420 tccatgggac tttccttccc tctcctgctt cctcttttcc tgctccctaa c 471 213 511 DNA Homo sapiens unsure (27) n=A,T,C or G 213 ctaattagaa acttgctgta ctttttnttt tcttttaggg gtcaaggacc ctctttatag 60 ctnccatttg cctacaataa attattgcag cagtttgcaa tactaaaata ttttttatag 120 actttatatt tttccttttg ataaagggat gctgcatagt agagttggtg taattaaact 180 atctcagccg tttccctgct ttcccttctg ctccatatgc ctcattgtcc ttccagggag 240 ctcttttaat cttaaagttc tacatttcat gctcttagtc aaattctgtt acctttttaa 300 taactcttcc cactgcatat ttccatcttg aattggnggt tctaaattct gaaactgtag 360 ttgagataca gctatttaat atttctggga gatgtgcatc cctcttcttt gtggttgccc 420 aaggttgttt tgcgtaactg anactccttg atatgcttca gagaatttag gcaaacactg 480 gccatggccg tgggagtact gggagtaaaa t 511 214 521 DNA Homo sapiens 214 agcattgcca aataatccct aattttccac taaaaatata atgaaatgat gttaagcttt 60 ttgaaaagtt taggttaaac ctactgttgt tagattaatg tatttgttgc ttccctttat 120 ctggaatgtg gcattagctt ttttatttta accctcttta attcttattc aattccatga 180 cttaaggttg gagagctaaa cactgggatt tttggataac agactgacag ttttgcataa 240 ttataatcgg cattgtacat agaaaggata tggctacctt ttgttaaatc tgcactttct 300 aaatatcaaa aaagggaaat gaagtataaa tcaatttttg tataatctgt ttgaaacatg 360 agttttattt gcttaatatt agggctttgc cccttttctg taagtctctt gggatcctgt 420 gtagaagctg ttctcattaa acaccaaaca gttaagtcca ttctctggta ctagctacaa 480 attcggtttc atattctact taacaattta aataaactga a 521 215 381 DNA Homo sapiens unsure (17) n=A,T,C or G 215 gagcggagag cggaccngtn agagccctga gcagccccac cgccgccgcc ggcctagttn 60 ncatcacacc ccgggaggag ccgcagctgc cgcagccggc cccagtcacc atcaccgcaa 120 ccatgagcag cgaggccgag acccagcagc cgcccgccgc cccccccgcc gcccccgccc 180 tcagcgccgc cgacaccaag cccggcacta cgggcagcgg cgcagggagc ggtggcccgg 240 gcggcctcac atcggcggcg cctgccggcg gggacaagaa ggtcatcgca acgaaggttt 300 tgggaacagt aaaatggttc aatgtaagga acggatatgg tttcatcaac aggaatgaca 360 ccaangaaga tgtatttgta c 381 216 425 DNA Homo sapiens 216 ttactaacta ggtcattcaa ggaagtcaag ttaacttaaa catgtcacct aaatgcactt 60 gatggtgttg aaatgtccac cttcttaaat ttttaagatg aacttagttc taaagaagat 120 aacaggccaa tcctgaaggt actccctgtt tgctgcagaa tgtcagatat tttggatgtt 180 gcataagagt cctatttgcc ccagttaatt caacttttgt ctgcctgttt tgtggactgg 240 ctggctctgt tagaactctg tccaaaaagt gcatggaata taacttgtaa agcttcccac 300 aattgacaat atatatgcat gtgtttaaac caaatccaga aagcttaaac aatagagctg 360 cataatagta tttattaaag aatcacaact gtaaacatga gaataactta aggattctag 420 tttag 425 217 181 DNA Homo sapiens 217 gagaaaccaa atgataggtt gtagagcctg atgactccaa acaaagccat cacccgcatt 60 cttcctcctt cttctggtgc tacagctcca agggcccttc accttcatgt ctgaaatgga 120 actttggctt tttcagtgga agaatatgtt gaaggtttca ttttgttcta gaaaaaaaaa 180 a 181 218 405 DNA Homo sapiens 218 caggccttcc agttcactga caaacatggg gaagtgtgcc cagctggctg gaaacctggc 60 agtgatacca tcaagcctga tgtccaaaag agcaaagaat atttctccaa gcagaagtga 120 gcgctgggct gttttagtgc caggctgcgg tgggcagcca tgagaacaaa acctcttctg 180 tatttttttt ttccattagt aaaacacaag acttcagatt cagccgaatt gtggtgtctt 240 acaaggcagg cctttcctac agggggtgga gagaccagcc tttcttcctt tggtaggaat 300 ggcctgagtt ggcgttgtgg gcaggctact ggtttgtatg atgtattagt agagcaaccc 360 attaatcttt tgtagtttgt attaaacttg aactgagaaa aaaaa 405 219 216 DNA Homo sapiens unsure (207) n=A,T,C or G 219 actccaagag ttagggcagc agagtggagc gatttagaaa gaacatttta aaacaatcag 60 ttaatttacc atgtaaaatt gctgtaaatg ataatgtgta cagattttct gttcaaatat 120 tcaattgtaa acttcttgtt aagactgtta cgtttctatt gcttttgtat gggatattgc 180 aaaaataaaa aggaaagaac cctcttnaan aaaaaa 216 220 380 DNA Homo sapiens 220 cttacaaatt gcccccatgt gtaggggaca cagaaccctt tgagaaaact tagatttttg 60 tctgtacaaa gtctttgcct ttttccttct tcattttttt ccagtacatt aaatttgtca 120 atttcatctt tgagggaaac tgattagatg ggttgtgttt gtgttctgat ggagaaaaca 180 gcaccccaag gactcagaag atgattttaa cagttcagaa cagatgtgtg caatattggt 240 gcatgtaata atgttgagtg gcagtcaaaa gtcatgattt ttatcttagt tcttcattac 300 tgcattgaaa aggaaaacct gtctgagaaa atgcctgaca gtttaattta aaactatggt 360 gtaagtcttt gacaaaaaaa 380 221 398 DNA Homo sapiens 221 ggttagtaag ctgtcgactt tgtaaaaaag ttaaaaatga aaaaaaaagg aaaaatgaat 60 tgtatattta atgaatgaac atgtacaatt tgccactggg aggaggttcc tttttgttgg 120 gtgagtctgc aagtgaattt cactgatgtt gatattcatt gtgtgtagtt ttatttcggt 180 cccagccccg tttcctttta ttttggagct aatgccagct gcgtgtctag ttttgagtgc 240 agtaaaatag aatcagcaaa tcactcttat ttttcatcct tttccggtat tttttgggtt 300 gtttctgtgg gagcagtgta caccaactct tcctgtatat tgcctttttg ctggaaaatg 360 ttgtatgttg aataaaattt tctataaaaa ttaaaaaa 398 222 301 DNA Homo sapiens unsure (49) n=A,T,C or G 222 ttcgataatt gatctcatgg gctttccctg gaggaaaggt tttttttgnt gtttattttt 60 taanaacttg aaacttgtaa actgagatgt ctgtagcttt tttgcccatc tgtagtgtat 120 gtgaagattt caaaacctga gagcactttt tctttgttta gaattatgag aaaggcacta 180 gatgacttta ggatttgcat ttttcccttt attgcctcat ttcttgtgac gccttgttgg 240 ggagggaaat ctgtttattt tttcctacaa ataaaaagct aagattctat atcgcaaaaa 300 a 301 223 200 DNA Homo sapiens 223 gtaagtgctt aggaagaaac tttgcaaaca tttaatgagg atacactgtt catttttaaa 60 attccttcac actgtaattt aatgtgtttt atattctttt gtagtaaaac aacataactc 120 agatttctac aggagacagt ggttttattt ggattgtctt ctgtaatagg tttcaataaa 180 gctggatgaa cttaaaaaaa 200 224 385 DNA Homo sapiens 224 gaaaggtttg atccggactc aaagaaagca aaggagtgtg agccgccatc tgctggagca 60 gctgtaactg caagacctgg acaagagatt cgtcagcgaa ctgcagctca aagaaacctt 120 tctccaacac cagcaagccc taaccagggc cctcctccac aagttccagt atctcctgga 180 ccaccaaagg acagttctgc ccctggtgga cccccagaaa ggactgttac tccagcccta 240 tcatcaaatg tgttaccaag acatcttgga tcccctgcta cttcagtgcc tggaatgggt 300 aaacagagca cttaatgtta tttacagttt atattgtttt ctctggttac caataaaacg 360 ggccattttc aggtggtaaa aaaaa 385 225 560 PRT Homo sapien 225 Met Glu Cys Leu Tyr Tyr Phe Leu Gly Phe Leu Leu Leu Ala Ala Arg 1 5 10 15 Leu Pro Leu Asp Ala Ala Lys Arg Phe His Asp Val Leu Gly Asn Glu 20 25 30 Arg Pro Ser Ala Tyr Met Arg Glu His Asn Gln Leu Asn Gly Trp Ser 35 40 45 Ser Asp Glu Asn Asp Trp Asn Glu Lys Leu Tyr Pro Val Trp Lys Arg 50 55 60 Gly Asp Met Arg Trp Lys Asn Ser Trp Lys Gly Gly Arg Val Gln Ala 65 70 75 80 Val Leu Thr Ser Asp Ser Pro Ala Leu Val Gly Ser Asn Ile Thr Phe 85 90 95 Ala Val Asn Leu Ile Phe Pro Arg Cys Gln Lys Glu Asp Ala Asn Gly 100 105 110 Asn Ile Val Tyr Glu Lys Asn Cys Arg Asn Glu Ala Gly Leu Ser Ala 115 120 125 Asp Pro Tyr Val Tyr Asn Trp Thr Ala Trp Ser Glu Asp Ser Asp Gly 130 135 140 Glu Asn Gly Thr Gly Gln Ser His His Asn Val Phe Pro Asp Gly Lys 145 150 155 160 Pro Phe Pro His His Pro Gly Trp Arg Arg Trp Asn Phe Ile Tyr Val 165 170 175 Phe His Thr Leu Gly Gln Tyr Phe Gln Lys Leu Gly Arg Cys Ser Val 180 185 190 Arg Val Ser Val Asn Thr Ala Asn Val Thr Leu Gly Pro Gln Leu Met 195 200 205 Glu Val Thr Val Tyr Arg Arg His Gly Arg Ala Tyr Val Pro Ile Ala 210 215 220 Gln Val Lys Asp Val Tyr Val Val Thr Asp Gln Ile Pro Val Phe Val 225 230 235 240 Thr Met Phe Gln Lys Asn Asp Arg Asn Ser Ser Asp Glu Thr Phe Leu 245 250 255 Lys Asp Leu Pro Ile Met Phe Asp Val Leu Ile His Asp Pro Ser His 260 265 270 Phe Leu Asn Tyr Ser Thr Ile Asn Tyr Lys Trp Ser Phe Gly Asp Asn 275 280 285 Thr Gly Leu Phe Val Ser Thr Asn His Thr Val Asn His Thr Tyr Val 290 295 300 Leu Asn Gly Thr Phe Ser Leu Asn Leu Thr Val Lys Ala Ala Ala Pro 305 310 315 320 Gly Pro Cys Pro Pro Pro Pro Pro Pro Pro Arg Pro Ser Lys Pro Thr 325 330 335 Pro Ser Leu Gly Pro Ala Gly Asp Asn Pro Leu Glu Leu Ser Arg Ile 340 345 350 Pro Asp Glu Asn Cys Gln Ile Asn Arg Tyr Gly His Phe Gln Ala Thr 355 360 365 Ile Thr Ile Val Glu Gly Ile Leu Glu Val Asn Ile Ile Gln Met Thr 370 375 380 Asp Val Leu Met Pro Val Pro Trp Pro Glu Ser Ser Leu Ile Asp Phe 385 390 395 400 Val Val Thr Cys Gln Gly Ser Ile Pro Thr Glu Val Cys Thr Ile Ile 405 410 415 Ser Asp Pro Thr Cys Glu Ile Thr Gln Asn Thr Val Cys Ser Pro Val 420 425 430 Asp Val Asp Glu Met Cys Leu Leu Thr Val Arg Arg Thr Phe Asn Gly 435 440 445 Ser Gly Thr Tyr Cys Val Asn Leu Thr Leu Gly Asp Asp Thr Ser Leu 450 455 460 Ala Leu Thr Ser Thr Leu Ile Ser Val Pro Asp Arg Asp Pro Ala Ser 465 470 475 480 Pro Leu Arg Met Ala Asn Ser Ala Leu Ile Ser Val Gly Cys Leu Ala 485 490 495 Ile Phe Val Thr Val Ile Ser Leu Leu Val Tyr Lys Lys His Lys Glu 500 505 510 Tyr Asn Pro Ile Glu Asn Ser Pro Gly Asn Val Val Arg Ser Lys Gly 515 520 525 Leu Ser Val Phe Leu Asn Arg Ala Lys Ala Val Phe Phe Pro Gly Asn 530 535 540 Gln Glu Lys Asp Pro Leu Leu Lys Asn Gln Glu Phe Lys Gly Val Ser 545 550 555 560 226 9 PRT Homo sapien 226 Ile Leu Ile Pro Ala Thr Trp Lys Ala 1 5 227 9 PRT Homo sapien 227 Phe Leu Leu Asn Asp Asn Leu Thr Ala 1 5 228 9 PRT Homo sapien 228 Leu Leu Gly Asn Cys Leu Pro Thr Val 1 5 229 10 PRT Homo sapien 229 Lys Leu Leu Gly Asn Cys Leu Pro Thr Val 1 5 10 230 10 PRT Homo sapien 230 Arg Leu Thr Gly Gly Leu Lys Phe Phe Val 1 5 10 231 9 PRT Homo sapien 231 Ser Leu Gln Ala Leu Lys Val Thr Val 1 5 232 20 PRT Homo sapiens 232 Ala Gly Ala Asp Val Ile Lys Asn Asp Gly Ile Tyr Ser Arg Tyr Phe 5 10 15 Phe Ser Phe Ala 20 233 21 PRT Homo sapiens 233 Phe Phe Ser Phe Ala Ala Asn Gly Arg Tyr Ser Leu Lys Val His Val 5 10 15 Asn His Ser Pro Ser 20 234 20 PRT Homo sapiens 234 Phe Leu Val Thr Trp Gln Ala Ser Gly Pro Pro Glu Ile Ile Leu Phe 5 10 15 Asp Pro Asp Gly 20 235 20 PRT Homo sapiens 235 Leu Gln Ser Ala Val Ser Asn Ile Ala Gln Ala Pro Leu Phe Ile Pro 5 10 15 Pro Asn Ser Asp 20 236 20 PRT Homo sapiens 236 Ile Gln Asp Asp Phe Asn Asn Ala Ile Leu Val Asn Thr Ser Lys Arg 5 10 15 Asn Pro Gln Gln 20 237 21 PRT Homo sapiens 237 Arg Asn Ser Leu Gln Ser Ala Val Ser Asn Ile Ala Gln Ala Pro Leu 5 10 15 Phe Ile Pro Pro Asn 20 238 20 PRT Homo sapiens 238 Thr His Glu Ser His Arg Ile Tyr Val Ala Ile Arg Ala Met Asp Arg 5 10 15 Asn Ser Leu Gln 20 239 20 PRT Homo sapiens 239 Arg Asn Pro Gln Gln Ala Gly Ile Arg Glu Ile Phe Thr Phe Ser Pro 5 10 15 Gln Ile Ser Thr 20 240 21 PRT Homo sapiens 240 Gly Gln Ala Thr Ser Tyr Glu Ile Arg Met Ser Lys Ser Leu Gln Asn 5 10 15 Ile Gln Asp Asp Phe 20 241 20 PRT Homo sapiens 241 Glu Arg Lys Trp Gly Phe Ser Arg Val Ser Ser Gly Gly Ser Phe Ser 5 10 15 Val Leu Gly Val 20 242 20 PRT Homo sapiens 242 Gly Ser His Ala Met Tyr Val Pro Gly Tyr Thr Ala Asn Gly Asn Ile 5 10 15 Gln Met Asn Ala 20 243 20 PRT Homo sapiens 243 Val Asn His Ser Pro Ser Ile Ser Thr Pro Ala His Ser Ile Pro Gly 5 10 15 Ser His Ala Met 20 244 20 PRT Homo sapiens 244 Ala Val Pro Pro Ala Thr Val Glu Ala Phe Val Glu Arg Asp Ser Leu 5 10 15 His Phe Pro His 20 245 20 PRT Homo sapiens 245 Lys Pro Gly His Trp Thr Tyr Thr Leu Asn Asn Thr His His Ser Leu 5 10 15 Gln Ala Leu Lys 20 246 20 PRT Homo sapiens 246 Asn Leu Thr Phe Arg Thr Ala Ser Leu Trp Ile Pro Gly Thr Ala Lys 5 10 15 Pro Gly His Trp 20 247 20 PRT Homo sapiens 247 Leu His Phe Pro His Pro Val Met Ile Tyr Ala Asn Val Lys Gln Gly 5 10 15 Phe Tyr Pro Ile 20 248 20 PRT Homo sapiens 248 Pro Glu Thr Gly Asp Pro Val Thr Leu Arg Leu Leu Asp Asp Gly Ala 5 10 15 Gly Ala Asp Val 20 249 20 PRT Homo sapiens 249 Gly Phe Tyr Pro Ile Leu Asn Ala Thr Val Thr Ala Thr Val Glu Pro 5 10 15 Glu Thr Gly Asp 20 250 20 PRT Homo sapiens 250 Phe Asp Pro Asp Gly Arg Lys Tyr Tyr Thr Asn Asn Phe Ile Thr Asn 5 10 15 Leu Thr Phe Arg 20 251 20 PRT Homo sapiens 251 Leu Gln Ala Leu Lys Val Thr Val Thr Ser Arg Ala Ser Asn Ser Ala 5 10 15 Val Pro Pro Ala 20 252 153 PRT Homo sapien 252 Met Ala Ser Val Arg Val Ala Ala Tyr Phe Glu Asn Phe Leu Ala Ala 1 5 10 15 Trp Arg Pro Val Lys Ala Ser Asp Gly Asp Tyr Tyr Thr Leu Ala Val 20 25 30 Pro Met Gly Asp Val Pro Met Asp Gly Ile Ser Val Ala Asp Ile Gly 35 40 45 Ala Ala Val Ser Ser Ile Phe Asn Ser Pro Glu Glu Phe Leu Gly Lys 50 55 60 Ala Val Gly Leu Ser Ala Glu Ala Leu Thr Ile Gln Gln Tyr Ala Asp 65 70 75 80 Val Leu Ser Lys Ala Leu Gly Lys Glu Val Arg Asp Ala Lys Ile Thr 85 90 95 Pro Glu Ala Phe Glu Lys Leu Gly Phe Pro Ala Ala Lys Glu Ile Ala 100 105 110 Asn Met Cys Arg Phe Tyr Glu Met Lys Pro Asp Arg Asp Val Asn Leu 115 120 125 Thr His Gln Leu Asn Pro Lys Val Lys Ser Phe Ser Gln Phe Ile Ser 130 135 140 Glu Asn Gln Gly Ala Phe Lys Gly Met 145 150 253 462 DNA Homo sapien 253 atggccagtg tccgcgtggc ggcctacttt gaaaactttc tcgcggcgtg gcggcccgtg 60 aaagcctctg atggagatta ctacaccttg gctgtaccga tgggagatgt accaatggat 120 ggtatctctg ttgctgatat tggagcagcc gtctctagca tttttaattc tccagaggaa 180 tttttaggca aggccgtggg gctcagtgca gaagcactaa caatacagca atatgctgat 240 gttttgtcca aggctttggg gaaagaagtc cgagatgcaa agattacccc ggaagctttc 300 gagaagctgg gattccctgc agcaaaggaa atagccaata tgtgtcgttt ctatgaaatg 360 aagccagacc gagatgtcaa tctcacccac caactaaatc ccaaagtcaa aagcttcagc 420 cagtttatct cagagaacca gggagccttc aagggcatgt ag 462 254 8031 DNA Homo sapien 254 tggcgaatgg gacgcgccct gtagcggcgc attaagcgcg gcgggtgtgg tggttacgcg 60 cagcgtgacc gctacacttg ccagcgccct agcgcccgct cctttcgctt tcttcccttc 120 ctttctcgcc acgttcgccg gctttccccg tcaagctcta aatcgggggc tccctttagg 180 gttccgattt agtgctttac ggcacctcga ccccaaaaaa cttgattagg gtgatggttc 240 acgtagtggg ccatcgccct gatagacggt ttttcgccct ttgacgttgg agtccacgtt 300 ctttaatagt ggactcttgt tccaaactgg aacaacactc aaccctatct cggtctattc 360 ttttgattta taagggattt tgccgatttc ggcctattgg ttaaaaaatg agctgattta 420 acaaaaattt aacgcgaatt ttaacaaaat attaacgttt acaatttcag gtggcacttt 480 tcggggaaat gtgcgcggaa cccctatttg tttatttttc taaatacatt caaatatgta 540 tccgctcatg aattaattct tagaaaaact catcgagcat caaatgaaac tgcaatttat 600 tcatatcagg attatcaata ccatattttt gaaaaagccg tttctgtaat gaaggagaaa 660 actcaccgag gcagttccat aggatggcaa gatcctggta tcggtctgcg attccgactc 720 gtccaacatc aatacaacct attaatttcc cctcgtcaaa aataaggtta tcaagtgaga 780 aatcaccatg agtgacgact gaatccggtg agaatggcaa aagtttatgc atttctttcc 840 agacttgttc aacaggccag ccattacgct cgtcatcaaa atcactcgca tcaaccaaac 900 cgttattcat tcgtgattgc gcctgagcga gacgaaatac gcgatcgctg ttaaaaggac 960 aattacaaac aggaatcgaa tgcaaccggc gcaggaacac tgccagcgca tcaacaatat 1020 tttcacctga atcaggatat tcttctaata cctggaatgc tgttttcccg gggatcgcag 1080 tggtgagtaa ccatgcatca tcaggagtac ggataaaatg cttgatggtc ggaagaggca 1140 taaattccgt cagccagttt agtctgacca tctcatctgt aacatcattg gcaacgctac 1200 ctttgccatg tttcagaaac aactctggcg catcgggctt cccatacaat cgatagattg 1260 tcgcacctga ttgcccgaca ttatcgcgag cccatttata cccatataaa tcagcatcca 1320 tgttggaatt taatcgcggc ctagagcaag acgtttcccg ttgaatatgg ctcataacac 1380 cccttgtatt actgtttatg taagcagaca gttttattgt tcatgaccaa aatcccttaa 1440 cgtgagtttt cgttccactg agcgtcagac cccgtagaaa agatcaaagg atcttcttga 1500 gatccttttt ttctgcgcgt aatctgctgc ttgcaaacaa aaaaaccacc gctaccagcg 1560 gtggtttgtt tgccggatca agagctacca actctttttc cgaaggtaac tggcttcagc 1620 agagcgcaga taccaaatac tgtccttcta gtgtagccgt agttaggcca ccacttcaag 1680 aactctgtag caccgcctac atacctcgct ctgctaatcc tgttaccagt ggctgctgcc 1740 agtggcgata agtcgtgtct taccgggttg gactcaagac gatagttacc ggataaggcg 1800 cagcggtcgg gctgaacggg gggttcgtgc acacagccca gcttggagcg aacgacctac 1860 accgaactga gatacctaca gcgtgagcta tgagaaagcg ccacgcttcc cgaagggaga 1920 aaggcggaca ggtatccggt aagcggcagg gtcggaacag gagagcgcac gagggagctt 1980 ccagggggaa acgcctggta tctttatagt cctgtcgggt ttcgccacct ctgacttgag 2040 cgtcgatttt tgtgatgctc gtcagggggg cggagcctat ggaaaaacgc cagcaacgcg 2100 gcctttttac ggttcctggc cttttgctgg ccttttgctc acatgttctt tcctgcgtta 2160 tcccctgatt ctgtggataa ccgtattacc gcctttgagt gagctgatac cgctcgccgc 2220 agccgaacga ccgagcgcag cgagtcagtg agcgaggaag cggaagagcg cctgatgcgg 2280 tattttctcc ttacgcatct gtgcggtatt tcacaccgca tatatggtgc actctcagta 2340 caatctgctc tgatgccgca tagttaagcc agtatacact ccgctatcgc tacgtgactg 2400 ggtcatggct gcgccccgac acccgccaac acccgctgac gcgccctgac gggcttgtct 2460 gctcccggca tccgcttaca gacaagctgt gaccgtctcc gggagctgca tgtgtcagag 2520 gttttcaccg tcatcaccga aacgcgcgag gcagctgcgg taaagctcat cagcgtggtc 2580 gtgaagcgat tcacagatgt ctgcctgttc atccgcgtcc agctcgttga gtttctccag 2640 aagcgttaat gtctggcttc tgataaagcg ggccatgtta agggcggttt tttcctgttt 2700 ggtcactgat gcctccgtgt aagggggatt tctgttcatg ggggtaatga taccgatgaa 2760 acgagagagg atgctcacga tacgggttac tgatgatgaa catgcccggt tactggaacg 2820 ttgtgagggt aaacaactgg cggtatggat gcggcgggac cagagaaaaa tcactcaggg 2880 tcaatgccag cgcttcgtta atacagatgt aggtgttcca cagggtagcc agcagcatcc 2940 tgcgatgcag atccggaaca taatggtgca gggcgctgac ttccgcgttt ccagacttta 3000 cgaaacacgg aaaccgaaga ccattcatgt tgttgctcag gtcgcagacg ttttgcagca 3060 gcagtcgctt cacgttcgct cgcgtatcgg tgattcattc tgctaaccag taaggcaacc 3120 ccgccagcct agccgggtcc tcaacgacag gagcacgatc atgcgcaccc gtggggccgc 3180 catgccggcg ataatggcct gcttctcgcc gaaacgtttg gtggcgggac cagtgacgaa 3240 ggcttgagcg agggcgtgca agattccgaa taccgcaagc gacaggccga tcatcgtcgc 3300 gctccagcga aagcggtcct cgccgaaaat gacccagagc gctgccggca cctgtcctac 3360 gagttgcatg ataaagaaga cagtcataag tgcggcgacg atagtcatgc cccgcgccca 3420 ccggaaggag ctgactgggt tgaaggctct caagggcatc ggtcgagatc ccggtgccta 3480 atgagtgagc taacttacat taattgcgtt gcgctcactg cccgctttcc agtcgggaaa 3540 cctgtcgtgc cagctgcatt aatgaatcgg ccaacgcgcg gggagaggcg gtttgcgtat 3600 tgggcgccag ggtggttttt cttttcacca gtgagacggg caacagctga ttgcccttca 3660 ccgcctggcc ctgagagagt tgcagcaagc ggtccacgct ggtttgcccc agcaggcgaa 3720 aatcctgttt gatggtggtt aacggcggga tataacatga gctgtcttcg gtatcgtcgt 3780 atcccactac cgagatatcc gcaccaacgc gcagcccgga ctcggtaatg gcgcgcattg 3840 cgcccagcgc catctgatcg ttggcaacca gcatcgcagt gggaacgatg ccctcattca 3900 gcatttgcat ggtttgttga aaaccggaca tggcactcca gtcgccttcc cgttccgcta 3960 tcggctgaat ttgattgcga gtgagatatt tatgccagcc agccagacgc agacgcgccg 4020 agacagaact taatgggccc gctaacagcg cgatttgctg gtgacccaat gcgaccagat 4080 gctccacgcc cagtcgcgta ccgtcttcat gggagaaaat aatactgttg atgggtgtct 4140 ggtcagagac atcaagaaat aacgccggaa cattagtgca ggcagcttcc acagcaatgg 4200 catcctggtc atccagcgga tagttaatga tcagcccact gacgcgttgc gcgagaagat 4260 tgtgcaccgc cgctttacag gcttcgacgc cgcttcgttc taccatcgac accaccacgc 4320 tggcacccag ttgatcggcg cgagatttaa tcgccgcgac aatttgcgac ggcgcgtgca 4380 gggccagact ggaggtggca acgccaatca gcaacgactg tttgcccgcc agttgttgtg 4440 ccacgcggtt gggaatgtaa ttcagctccg ccatcgccgc ttccactttt tcccgcgttt 4500 tcgcagaaac gtggctggcc tggttcacca cgcgggaaac ggtctgataa gagacaccgg 4560 catactctgc gacatcgtat aacgttactg gtttcacatt caccaccctg aattgactct 4620 cttccgggcg ctatcatgcc ataccgcgaa aggttttgcg ccattcgatg gtgtccggga 4680 tctcgacgct ctcccttatg cgactcctgc attaggaagc agcccagtag taggttgagg 4740 ccgttgagca ccgccgccgc aaggaatggt gcatgcaagg agatggcgcc caacagtccc 4800 ccggccacgg ggcctgccac catacccacg ccgaaacaag cgctcatgag cccgaagtgg 4860 cgagcccgat cttccccatc ggtgatgtcg gcgatatagg cgccagcaac cgcacctgtg 4920 gcgccggtga tgccggccac gatgcgtccg gcgtagagga tcgagatctc gatcccgcga 4980 aattaatacg actcactata ggggaattgt gagcggataa caattcccct ctagaaataa 5040 ttttgtttaa ctttaagaag gagatataca tatgcagcat caccaccatc accacggagt 5100 acagcttcaa gacaatgggt ataatggatt gctcattgca attaatcctc aggtacctga 5160 gaatcagaac ctcatctcaa acattaagga aatgataact gaagcttcat tttacctatt 5220 taatgctacc aagagaagag tatttttcag aaatataaag attttaatac ctgccacatg 5280 gaaagctaat aataacagca aaataaaaca agaatcatat gaaaaggcaa atgtcatagt 5340 gactgactgg tatggggcac atggagatga tccatacacc ctacaataca gagggtgtgg 5400 aaaagaggga aaatacattc atttcacacc taatttccta ctgaatgata acttaacagc 5460 tggctacgga tcacgaggcc gagtgtttgt ccatgaatgg gcccacctcc gttggggtgt 5520 gttcgatgag tataacaatg acaaaccttt ctacataaat gggcaaaatc aaattaaagt 5580 gacaaggtgt tcatctgaca tcacaggcat ttttgtgtgt gaaaaaggtc cttgccccca 5640 agaaaactgt attattagta agctttttaa agaaggatgc acctttatct acaatagcac 5700 ccaaaatgca actgcatcaa taatgttcat gcaaagttta tcttctgtgg ttgaattttg 5760 taatgcaagt acccacaacc aagaagcacc aaacctacag aaccagatgt gcagcctcag 5820 aagtgcatgg gatgtaatca cagactctgc tgactttcac cacagctttc ccatgaacgg 5880 gactgagctt ccacctcctc ccacattctc gcttgtagag gctggtgaca aagtggtctg 5940 tttagtgctg gatgtgtcca gcaagatggc agaggctgac agactccttc aactacaaca 6000 agccgcagaa ttttatttga tgcagattgt tgaaattcat accttcgtgg gcattgccag 6060 tttcgacagc aaaggagaga tcagagccca gctacaccaa attaacagca atgatgatcg 6120 aaagttgctg gtttcatatc tgcccaccac tgtatcagct aaaacagaca tcagcatttg 6180 ttcagggctt aagaaaggat ttgaggtggt tgaaaaactg aatggaaaag cttatggctc 6240 tgtgatgata ttagtgacca gcggagatga taagcttctt ggcaattgct tacccactgt 6300 gctcagcagt ggttcaacaa ttcactccat tgccctgggt tcatctgcag ccccaaatct 6360 ggaggaatta tcacgtctta caggaggttt aaagttcttt gttccagata tatcaaactc 6420 caatagcatg attgatgctt tcagtagaat ttcctctgga actggagaca ttttccagca 6480 acatattcag cttgaaagta caggtgaaaa tgtcaaacct caccatcaat tgaaaaacac 6540 agtgactgtg gataatactg tgggcaacga cactatgttt ctagttacgt ggcaggccag 6600 tggtcctcct gagattatat tatttgatcc tgatggacga aaatactaca caaataattt 6660 tatcaccaat ctaacttttc ggacagctag tctttggatt ccaggaacag ctaagcctgg 6720 gcactggact tacaccctga acaataccca tcattctctg caagccctga aagtgacagt 6780 gacctctcgc gcctccaact cagctgtgcc cccagccact gtggaagcct ttgtggaaag 6840 agacagcctc cattttcctc atcctgtgat gatttatgcc aatgtgaaac agggatttta 6900 tcccattctt aatgccactg tcactgccac agttgagcca gagactggag atcctgttac 6960 gctgagactc cttgatgatg gagcaggtgc tgatgttata aaaaatgatg gaatttactc 7020 gaggtatttt ttctcctttg ctgcaaatgg tagatatagc ttgaaagtgc atgtcaatca 7080 ctctcccagc ataagcaccc cagcccactc tattccaggg agtcatgcta tgtatgtacc 7140 aggttacaca gcaaacggta atattcagat gaatgctcca aggaaatcag taggcagaaa 7200 tgaggaggag cgaaagtggg gctttagccg agtcagctca ggaggctcct tttcagtgct 7260 gggagttcca gctggccccc accctgatgt gtttccacca tgcaaaatta ttgacctgga 7320 agctgtaaaa gtagaagagg aattgaccct atcttggaca gcacctggag aagactttga 7380 tcagggccag gctacaagct atgaaataag aatgagtaaa agtctacaga atatccaaga 7440 tgactttaac aatgctattt tagtaaatac atcaaagcga aatcctcagc aagctggcat 7500 cagggagata tttacgttct caccccaaat ttccacgaat ggacctgaac atcagccaaa 7560 tggagaaaca catgaaagcc acagaattta tgttgcaata cgagcaatgg ataggaactc 7620 cttacagtct gctgtatcta acattgccca ggcgcctctg tttattcccc ccaattctga 7680 tcctgtacct gccagagatt atcttatatt gaaaggagtt ttaacagcaa tgggtttgat 7740 aggaatcatt tgccttatta tagttgtgac acatcatact ttaagcagga aaaagagagc 7800 agacaagaaa gagaatggaa caaaattatt ataatgaatt ctgcagatat ccatcacact 7860 ggcggccgct cgagcaccac caccaccacc actgagatcc ggctgctaac aaagcccgaa 7920 aggaagctga gttggctgct gccaccgctg agcaataact agcataaccc cttggggcct 7980 ctaaacgggt cttgaggggt tttttgctga aaggaggaac tatatccgga t 8031 255 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 255 gtggccagng actagaaggc gaggcgccgc gggaccatgg cggcggcggc ggacgagcgg 60 agtccanagg acggagaaga cgaggaagag gaggagcagt tggttctggt ggaattatca 120 ggaattattg attcagactt cctctcaaaa tgtgaaaata aatgcaaggt tttgggcatt 180 gacactgaga ggcccattct gcaagtggac agctgtgtct ttgctgggga gtatgaagac 240 actctangga cctgtgttat atttgaagaa aatgntnaac atgctgatac agaaggcaat 300 aataaaacag tgctaaaata taaatgccat acaatgaaga agctcagcat gacaagaact 360 ctcctgacag agaagaagga aggagaagaa aacatangtg g 401 256 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 256 tggtggncct gggatgggga accgcggtgg cttccgngga ggtttcggca ntggcatccg 60 gggccggggt cgcggccgng gacggggccg gggccnangc cgnnganctc gcggangcaa 120 ggccgaggat aaggagtgga tgcccgtcac caacttgggc cgcttgncca aggacatgaa 180 nancaagccc ctgnaggaga tctatntctt cttccctgcc ccattaagga atcaagagat 240 catttgattt cttcctgggg gcctctctca aggatnaggt ttttgaagat tatgccagtg 300 canaaannan accccgttgc ccngtccatc tncacccaac ncttccaagg gcnatttttg 360 tttaggcctc attncngggg ggaaccttaa cccaatttgg g 401 257 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 257 atgtatgtaa aacacttcat aaaatgtaaa gggctataac aaatatgtta taaagtgatt 60 ctctcagccc tgaggtatac agaatcattt gcctcagact gctgttggat tttaaaattt 120 ttaaaatatc tgctaagtaa tttgctatgt cttctcccac actatcaata tgcctgcttc 180 taacaggctc cccactttct tttaatgtgc tgttatgagc tttggacatg agataaccgt 240 gcctgttcag agtgtctaca gtaagagctg gacaaactct ggagggacac agtctttgag 300 acagctcttt tggttgcttt ccacttttct gaaaggttca cagtaacctt ctagataata 360 gaaactccca gttaaagcct angctancaa ttttttttag t 401 258 401 DNA Homo sapien 258 ggagcgctag gtcggtgtac gaccgagatt agggtgcgtg ccagctccgg gaggccgcgg 60 tgaggggccg ggcccaagct gccgacccga gccgatcgtc agggtcgcca gcgcctcagc 120 tctgtggagg agcagcagta gtcggagggt gcaggatatt agaaatggct actccccagt 180 caattttcat ctttgcaatc tgcattttaa tgataacaga attaattctg gcctcaaaaa 240 gctactatga tatcttaggt gtgccaaaat cggcatcaga gcgccaaatc aagaaggcct 300 ttcacaagtt ggccatgaag taccaccctg acaaaaataa gacccagatg ctgaagcaaa 360 attcagagag attgcagaag catatgaaac actctcagat g 401 259 401 DNA Homo sapien 259 attgggtttg gagggaggat gatgacagag gaatgccctt tggccatcac ggttttgatt 60 ctccagaata ttgtgggttt gatcatcaat gcagtcatgt taggctgcat tttcatgaaa 120 acagctcagg ctcacagaag ggcagaaact ttgattttca gccgccatgc tgtgattgcc 180 gtccgaaatg gcaagctgtg cttcatgttc cgagtgggtg acctgaggaa aagcatgatc 240 attagtgcct ctgtgcgcat ccaggtggtc aagaaaacaa ctacacctga aggggaggtg 300 gttcctattc accaactgga cattcctgtt gataacccaa tcgagagcaa taacattttt 360 ctggtggccc ctttgatcat ctgccacgtg attgacaagc g 401 260 363 DNA Homo sapien misc_feature (1)...(363) n = A,T,C or G 260 aggaganang gagggggana tgaataggga tggagaggga natagtggat gagcagggca 60 canggagagg aancagaaag gagaggcaag acagggagac acacancaca nangangana 120 caggtggggg ctggggtggg gcatggagag cctttnangt cncccaggcc accctgctct 180 cgctggnctg ttgaaaccca ctccatggct tcctgccact gcagttgggc ccagggctgg 240 cttattnctg gaatgcaagt ggctgtggct tggagcctcc cctctggnnn anggaaannn 300 attgctccct tatctgcttg gaatatctga gtttttccan cccggaaata aaacacacac 360 aca 363 261 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 261 cggctctccg ccgctctccc ggggtttcgg ggcacttggg tcccacagtc tggtcctgct 60 tcaccttccc ctgacctgag tagtcgccat ggcacaggtt ctcagaggca ctgngactga 120 cttccctgga tttgatgagc gggctgatgc anaaactctt cggaaggcta tgaaaggctt 180 gggcacagat gaggagagca tcctgactct gttgacatcc cgaagtaatg ctcagcgcca 240 ggaaatctct gcagctttta agactctgtt tggcagggat cttctggatg acctgaaatc 300 agaactaact ggaaaatttg aaaaattaat tgtggctctg atgaaaccct ctcggcttta 360 tgatgcttat gaactgaaac atgccttgaa gggagctgga a 401 262 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 262 agtctanaac atttctaata ttttgngctt tcatatatca aaggagatta tgtgaaacta 60 tttttaaata ctgtaaagtg acatatagtt ataagatata tttctgtaca gtagagaaag 120 agtttataac atgaagaata ttgtaccatt atacattttc attctcgatc tcataagaaa 180 ttcaaaagaa taatgataga ggtgaaaata tgtttacttt ctctaaatca agcctagttg 240 tcaactcaaa aattatgntg catagtttta ttttgaattt aggttttggg actacttttt 300 tccancttca atgagaaaat aaaatctaca actcaggagt tactacagaa gttctaanta 360 tttttttgct aannagcnaa aaatataaac atatgaaaat g 401 263 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 263 ctgtccgacc aagagaggcc ggccgagccc gaggcttggg cttttgcttt ctggcggagg 60 gatctgcggc ggtttaggag gcggcgctga tcctgggagg aagaggcagc tacggcggcg 120 gcggcggtgg cggctagggc ggcggcgaat aaaggggccg ccgccgggtg atgcggtgac 180 cactgcggca ggcccaggag ctgagtgggc cccggccctc agcccgtccc gncggacccg 240 ctttcctcaa ctctccatct tctcctgccg accgagatcg ccgaggcggn ctcaggctcc 300 ctancccctt ccccgtccct tccccncccc cgtccccgcc ccgggggccg ccgccacccg 360 cctcccacca tggctctgaa ganaatccac aaggaattga a 401 264 401 DNA Homo sapien 264 aacaccagcc actccaggac ccctgaaggc ctctaccagg tcaccagtgt tctgcgccta 60 aagccacccc ctggcagaaa cttcagctgt gtgttctgga atactcacgt gagggaactt 120 actttggcca gcattgacct tcaaagtcag atggaaccca ggacccatcc aacttggctg 180 cttcacattt tcatcccctc ctgcatcatt gctttcattt tcatagccac agtgatagcc 240 ctaagaaaac aactctgtca aaagctgtat tcttcaaaag acacaacaaa aagacctgtc 300 accacaacaa agagggaagt gaacagtgct gtgaatctga acctgtggtc ttgggagcca 360 gggtgacctg atatgacatc taaagaagct tctggactct g 401 265 271 DNA Homo sapien misc_feature (1)...(271) n = A,T,C or G 265 gccacttcct gtggacatgg gcagagcgct gctgccagtt cctggtagcc ttgaccacna 60 cgctgggggg tctttgtgat ggtcatgggt ctcatttgca cttgggggtg tgggattcaa 120 gttagaagtt tctagatctg gccgggcgca gtggctcaca cctgtaatcc cagcacttta 180 ggaggctgag gcaggcggat catgaggtca ggagatcgag accgtcctgg ctaacacagt 240 gaaaccccgt ctctactaaa aatacaaaaa a 271 266 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 266 attcataaat ttagctgaaa gatactgatt caatttgtat acagngaata taaatgagac 60 gacagcaaaa ttttcatgaa atgtaaaata tttttatagt ttgttcatac tatatgaggt 120 tctattttaa atgactttct ggattttaaa aaatttcttt aaatacaatc atttttgtaa 180 tatttatttt atgcttatga tctagataat tgcagaatat cattttatct gactctgtct 240 tcataagaga gctgtggccg aattttgaac atctgttata gggagtgatc aaattagaag 300 gcaatgtgga aaaacaattc tgggaaagat ttctttatat gaagtccctg ccactagcca 360 gccatcctaa ttgatgaaag ttatctgttc acaggcctgc a 401 267 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 267 gaagaggcat cacctgatcc cggagacctt tggagttaag aggcggcgga agcgagggcc 60 tgtggagtcg gatcctcttc ggggtgagcc agggtcggcg cgcgcggctg tctcanaact 120 catgcagctg ttcccgcgag gcctgtttga ggacgcgctg ccgcccatcg tgctgaggag 180 ccaggtgtac agccttgtgc ctgacaggac cgtggccgac cggcagctga aggagcttca 240 agagcanggg gagacaaaat cgtccagctg ggcttcnact tggatgccca tggaanttat 300 tctttcnctt ganggactta cnngggaccc aagaanccct tncaaggggc ccttngtgga 360 tgggncccga aaccccnnta tttgcccttg ggggggncca a 401 268 223 DNA Homo sapien 268 tcgccatgtt ggccaggctg gtcttgaact cctgacttta agtgatccac ccgcctcaac 60 ctcccaaagt gctgggatta caggtgtgag ccaccgcgcc tggcctgata catactttta 120 gaatcaagta gtcacgcact ttttctgttc atttttctaa aaagtaaata tacaaatgtt 180 ttgttttttg ttttttttgt ttgtttgttt ctgttttttt ttt 223 269 401 DNA Homo sapien 269 actatgtaaa ccacattgta ctttttttta ctttggcaac aaatatttat acatacaaga 60 tgctagttca tttgaatatt tctcccaact tatccaagga tctccagctc taacaaaatg 120 gtttattttt atttaaatgt caatagttgt tttttaaaat ccaaatcaga ggtgcaggcc 180 accagttaaa tgccgtctat caggttttgt gccttaagag actacagagt caaagctcat 240 ttttaaagga gtaggacaaa gttgtcacag gtttttgttg ttgtttttat tgcccccaaa 300 attacatgtt aatttccatt tatatcaggg attctattta cttgaagact gtgaagttgc 360 cattttgtct cattgttttc tttgacataa ctaggatcca t 401 270 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 270 tggctgttga ttcacctcag cactgcttgg tatctgcacc ctacctctct ttagaggctg 60 ccttgtcaac tgaaaaatgc acctgacttc gagcaagact ctttccttag gttctggatc 120 tgtttgagcc ccatggcact gagctggaat ctgagggtct tgttccaagg atgtgatgat 180 gtgggagaat gttctttgaa agagcagaaa tccagtctgc atggaaacag cctgtagagn 240 agaagtttcc agtgataagt gttcactgtt ctaaggaggt acaccacagc tacctgaatt 300 ttcccaaaat gagtgcttct gtgcgttaca actggccttt gtacttgact gtgatgactt 360 tgttttttct tttcaattct anatgaacat gggaaaaaat g 401 271 329 DNA Homo sapien 271 ccacagcctc caagtcaggt ggggtggagt cccagagctg cacagggttt ggcccaagtt 60 tctaagggag gcacttcctc ccctcgccca tcagtgccag cccctgctgg ctggtgcctg 120 agcccctcag acagccccct gccccgcagg cctgccttct cagggacttc tgcggggcct 180 gaggcaagcc atggagtgag acccaggagc cggacacttc tcaggaaatg gcttttccca 240 acccccagcc cccacccggt ggttcttcct gttctgtgac tgtgtatagt gccaccacag 300 cttatggcat ctcattgagg acaaaaaaa 329 272 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 272 nggctgntaa cntcggaggt nacttcctgg actatcctgg agaccccctc cgcttccacg 60 nncatnatat cnctcatngc tgggcccntn angacacnat cccactccaa cacctgngng 120 atgctggncn cctnggaacc ancntcagaa ngaccctgnt cntntgtnnt ccgcaanctg 180 aagnnaangc gggntacacc tncntgcant ggnccacnct gcngggaact ntacacacct 240 acgggatgtg gctgcgccan gagccaagag cntttctgga tgattcccca gcctcttgnn 300 agggantcta caacattgct nnntaccttt ntccnncngc nnntnntgga ntacaggngn 360 tnntaacact acatcttttt tactgcnccn tncttggtgg g 401 273 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 273 cagcaccatg aagatcaaga tcatcgcacc cccagagcgc aagtactcgg tgtggatcgg 60 tggctccatc ctggcctcac tgtccacctt ccagcagatg tggattagca agcaggagta 120 cgacgagtcg ggcccctcca tcgtccaccg caaatgcttc taaacggact cagcagatgc 180 gtagcatttg ctgcatgggt taattgagaa tagaaatttg cccctggcaa atgcacacac 240 ctcatgctag cctcacgaaa ctggaataag ccttcgaaaa gaaattgtcc ttgaagcttg 300 tatctgatat cagcactgga ttgtagaact tgttgctgat tttgaccttg tattgaagtt 360 aactgttccc cttggtatta acgtgtcagg gctgagtgnt c 401 274 401 DNA Homo sapien 274 ccacccacac ccaccgcgcc ctcgttcgcc tcttctccgg gagccagtcc gcgccaccgc 60 cgccgcccag gccatcgcca ccctccgcag ccatgtccac caggtccgtg tcctcgtcct 120 cctaccgcag gatgttcggc ggcccgggca ccgcgagccg gccgagctcc agccggagct 180 acgtgactac gtccacccgc acctacagcc tgggcagcgc gctgcgcccc agcaccagcc 240 gcagcctcta cgcctcgtcc ccgggcggcg tgtatgccac gcgctcctct gccgtgcgcc 300 tgcggagcag cgtgcccggg gtgcggctcc tgcaggactc ggtggacttc tcgctggccg 360 acgccatcaa caccgagttc aagaacaccc gcaccaacga g 401 275 401 DNA Homo sapien 275 ccacttccac cactttgtgg agcagtgcct tcagcgcaac ccggatgcca ggtatccctg 60 ctggcctggg cctgggcttc gggagagcag agggtgctca ggagggtaag gccagggtgt 120 gaagggactt acctcccaaa ggttctgcag gggaatctgg agctacacac aggagggatc 180 agctcctggg tgtgtcagag gccagcctgg ggagctctgg ccactgcttc ccatgagctg 240 agggagaggg agaggggacc cgaggctgag gcataagtgg caggatttcg ggaagctggg 300 gacacggcag tgatgctgcg gtctctcctc ccctttccct ccaggcccag tgccagcacc 360 ctcctgaacc actctttctt caagcagatc aagcgacgtg c 401 276 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 276 tctgatattg ntacccttga gccacctaag ttagaagaaa ttggaaatca agaagttgtc 60 attgttgaag aagcacagag ttcagaagac tttaacatgg gctcttcctc tagcagccag 120 tatactttct gtcagccaga aactgtattt tcatctcagc ctagtgatga tgaatcaagt 180 agtgatgaaa ccagtaatca gcccagtcct gcctttagac gacgccgtgc taggaagaag 240 accgtttctg cttcagaatc tgaagaccgg ctagttggtg aacaagaaac tgaaccttct 300 aaggagttga gtaaacgtca gttcagtagt ggtctcaata agtgtgttat acttgctttg 360 gtgattgcaa tcagcatggg atttggccat ttctatggca c 401 277 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 277 aactttggca acatatctca gcaaaaacta cagctatgtt attcatgcca aaataaaagc 60 tgtgcagagg agtggctgca atgaggtcac aacggtggtg gatgtaaaag agatcttcaa 120 gtcctcatca cccatccctc gaactcaagt cccgctcatt acaaattctt cttgccagtg 180 tccacacatc ctgccccatc aagatgttct catcatgtgt tacgagnggc gctcaaggat 240 gatgcttctt gaaaattgct tagttgaaaa atggagagat cagcttagta aaagatccat 300 acagtgggaa gagaggctgc aggaacagcg ganaacagtt caggacaaga agaaaacagc 360 cgggcgcacc agtcgtagta atccccccaa accaaaggga a 401 278 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 278 aatgagtgtg agaccacaaa tgaatgccgg gaggatgaaa tgtgttggaa ttatcatggc 60 ggcttccgtt gttatccacg aaatccttgt caagatccct acattctaac accagagaac 120 cgatgtgttt gcccagtctc aaatgccatg tgccgagaac tgccccagtc aatagtctac 180 aaatacatga gcatccgatc tgataggtct gtgccatcag acatcttcca gatacaggcc 240 acaactattt atgccaacac catcaatact tttcggatta aatctggaaa tgaaaatgga 300 gagtctacct acgacaacaa anccctgtaa gtgcaatgct tgtgctcgtg aagncattat 360 caggaccaag agaacatatc gtggacctgg agatgctgac a 401 279 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 279 aaattattgc ctctgataca tacctaagtn aacanaacat taatacctaa gtaaacataa 60 cattacttgg agggttgcag nttctaantg aaactgtatt tgaaactttt aagtatactt 120 taggaaacaa gcatgaacgg cagtctagaa taccagaaac atctacttgg gtagcttggn 180 gccattatcc tgtggaatct gatatgtctg gnagcatgtc attgatggga catgaagaca 240 tctttggaaa tgatgagatt atttcctgtg ttaaaaaaaa aaaaaatctt aaattcctac 300 aatgtgaaac tgaaactaat aattttgatc ctgatgtatg ggacagcgta tctgtaccag 360 gctctaaata acaaaagnta gggngacaag nacatgttcc t 401 280 326 DNA Homo sapien 280 gaagtggaat tgtataattc aattcgataa ttgatctcat gggctttccc tggaggaaag 60 gttttttttg ttgttttttt tttaagaact tgaaacttgt aaactgagat gtctgtagct 120 tttttgccca tctgtagtgt atgtgaagat ttcaaaacct gagagcactt tttctttgtt 180 tagaattatg agaaaggcac tagatgactt taggatttgc atttttccct ttattgcctc 240 atttcttgtg acgccttgtt ggggagggaa atctgtttat tttttcctac aaataaaaag 300 ctaagattct atatcgcaaa aaaaaa 326 281 374 DNA Homo sapien 281 caacgcgttt gcaaatattc ccctggtagc ctacttcctt acccccgaat attggtaaga 60 tcgagcaatg gcttcaggac atgggttctc ttctcctgtg atcattcaag tgctcactgc 120 atgaagactg gcttgtctca gtgtttcaac ctcaccaggg ctgtctcttg gtccacacct 180 cgctccctgt tagtgccgta tgacagcccc catcaaatga ccttggccaa gtcacggttt 240 ctctgtggtc aaggttggtt ggctgattgg tggaaagtag ggtggaccaa aggaggccac 300 gtgagcagtc agcaccagtt ctgcaccagc agcgcctccg tcctagtggg tgttcctgtt 360 tctcctggcc ctgg 374 282 404 DNA Homo sapien misc_feature (1)...(404) n = A,T,C or G 282 agtgtggtgg aattcccgca tcctanncgc cgactcacac aaggcagagt ngccatggag 60 aaaattccag tgtcagcatt cttgctcctt gtggccctct cctacactct ggccagagat 120 accacagtca aacctgnagc caaaaaggac acaaaggact ctcgacccaa actgccccan 180 accctctcca gaggttgggg tgaccaactc atctggactc anacatatga agaagctcta 240 tataaatcca agacaagcaa caaacccttg atgattattc atcacttgga tgagtgccca 300 cacagtcaag ctttaaagaa agtgtttgct gaaaataaag aaatccagaa attggcagag 360 cagtttgtcc tcctcaatct ggtttatgaa acaactgaca aaca 404 283 184 DNA Homo sapien misc_feature (1)...(184) n = A,T,C or G 283 agtgtggtgg aattcacttg cttaanttgt gggcaaaaga gaaaaagaag gattgatcag 60 agcattgtgc aatacagttt cattaactcc ttccctcgct cccccaaaaa tttgaatttt 120 tttttcaaca ctcttacacc tgttatggaa aatgtcaacc tttgtaagaa aaccaaaata 180 aaaa 184 284 421 DNA Homo sapien misc_feature (1)...(421) n = A,T,C or G 284 ctattaatcc tgccacaata tttttaatta cgtacaaaga tctgacatgt cacccaggga 60 cccatttcac ccactgctct gtttggccgc cagtcttttg tctctctctt cagcaatggt 120 gaggcggata ccctttcctc ggggaanana aatccatggt ttgttgccct tgccaataac 180 aaaaatgttg gaaagtcgag tggcaaagct gttgccattg gcatctttca cgtgaaccac 240 gtcaaaagat ccagggtgcc tctctctgtt ggtgatcaca ccaattcttc ctaggttagc 300 acctccagtc accatacaca ggttaccagt gtcgaacttg atgaaatcag taatcttgcc 360 agtctctaaa tcaatctgaa tggtatcatt caccttgatg aggggatcgg ggtagcggat 420 g 421 285 361 DNA Homo sapien misc_feature (1)...(361) n = A,T,C or G 285 ctgggtggta actctttatt tcattgtccg gaanaaagat gggagtggga acagggtgga 60 cactgtgcag gcttcagctt ccactccggg caggattcag gctatctggg accgcaggga 120 ctgccaggtg cacagccctg gctcccgagg caggcaggca aggtgacggg actggaagcc 180 cttttcanag ccttggagga gctggtccgt ccacaagcaa tgagtgccac tctgcagttt 240 gcaggggatg gataaacagg gaaacactgt gcattcctca cagccaacag tgtaggtctt 300 ggtgaagccc cggcgctgag ctaagctcag gctgttccag ggagccacga aactgcaggt 360 a 361 286 336 DNA Homo sapien misc_feature (1)...(336) n = A,T,C or G 286 tttgagtggc agcgccttta tttgtggggg ccttcaaggn agggtcgtgg ggggcagcgg 60 ggaggaanag ccganaaact gtgtgaccgg ggcctcaggt ggtgggcatt gggggctcct 120 cttgcanatg cccattggca tcaccggtgc agccattggt ggcagcgggt accggtcctt 180 tcttgttcaa catagggtag gtggcagcca cgggtccaac tcgcttgagg ctgggccctg 240 ggcgctccat tttgtgttcc angagcatgt ggttctgtgg cgggagcccc acgcaggccc 300 tgaggatgtt ctcgatgcag ctgcgctggc ggaaaa 336 287 301 DNA Homo sapien misc_feature (1)...(301) n = A,T,C or G 287 tgggtaccaa atttntttat ttgaaggaat ggnacaaatc aaanaactta agnggatgtt 60 ttggtacaac ttatanaaaa ggnaaaggaa accccaacat gcatgcnctg ccttggngac 120 cagggaagtc accccacggc tatggggaaa ttancccgag gcttancttt cattatcact 180 gtctcccagg gngngcttgt caaaaanata ttccnccaag ccaaattcgg gcgctcccat 240 nttgcncaag ttggtcacgt ggtcacccaa ttctttgatg gctttcacct gctcattcag 300 g 301 288 358 DNA Homo sapien misc_feature (1)...(358) n = A,T,C or G 288 aagtttttaa actttttatt tgcatattaa aaaaattgng cattccaata attaaaatca 60 tttgaacaaa aaaaaaaatg gcactctgat taaactgcat tacagcctgc aggacacctt 120 gggccagctt ggttttactc tanatttcac tgtcgtccca ccccacttct tccaccccac 180 ttcttccttc accaacatgc aagttctttc cttccctgcc agccanatag atagacagat 240 gggaaaggca ggcgcggcct tcgttgtcag tagttctttg atgtgaaagg ggcagcacag 300 tcatttaaac ttgatccaac ctctttgcat cttacaaagt taaacagcta aaagaagt 358 289 462 DNA Homo sapien misc_feature (1)...(462) n = A,T,C or G 289 ggcatcagaa atgctgttta tttctctgct gctcccaagc tggctggcct ttgcagagga 60 gcagacaaca gatgcatagt tgggganaaa gggaggacag gttccaggat agagggtgca 120 ggctgaggga ggaagggtaa naggaaggaa ggccatcctg gatccccaca tttcagtctc 180 anatgaggac aaagggactc ccaagccccc aaatcatcan aaaacaccaa ggagcaggag 240 gagcttgagc aggccccagg gagcctcana gccataccag ccactgtcta cttcccatcc 300 tcctctccca ttccctgtct gcttcanacc acctcccagc taagccccag ctccattccc 360 ccaatcctgg cccttgccag cttgacagtc acagtgcctg gaattccacc actgaggctt 420 ctcccagttg gattaggacg tcgccctgtt agcatgctgc cc 462 290 481 DNA Homo sapien misc_feature (1)...(481) n = A,T,C or G 290 tactttccta aactttatta aagaaaaaag caataagcaa tggnggtaaa tctctanaac 60 atacccaatt ttctgggctt cctcccccga gaatgtgaca ttttgatttc caaacatgcc 120 anaagtgtat ggttcccaac tgtactaaag taggtganaa gctgaagtcc tcaagtgttc 180 atcttccaac ttttcccagt ctgtggtctg tctttggatc agcaataatt gcctgaacag 240 ctactatggc ttcgttgatt tttgtctgta gctctctgag ctcctctatg tgcagcaatc 300 gcanaatttg agcagcttca ttaanaactg catctcctgt gtcaaaacca anaatatgtt 360 tgtctaaagc aacaggtaag ccctcttttg tttgatttgc cttancaact gcatcctgtg 420 tcaggcgctc ctgaaccaaa atccgaattg ccttaagcat taccaggtaa tcatcatgac 480 g 481 291 381 DNA Homo sapien misc_feature (1)...(381) n = A,T,C or G 291 tcatagtaat gtaaaaccat ttgtttaatt ctaaatcaaa tcactttcac aacagtgaaa 60 attagtgact ggttaaggng tgccactgta catatcatca ttttctgact ggggtcagga 120 cctggtccta gtccacaagg gtggcaggag gagggtggag gctaanaaca cagaaaacac 180 acaaaanaaa ggaaagctgc cttggcanaa ggatgaggng gtgagcttgc cgaaggatgg 240 tgggaagggg gctccctgtt ggggccgagc caggagtccc aagtcagctc tcctgcctta 300 cttagctcct ggcanagggt gagtggggac ctacgaggtt caaaatcaaa tggcatttgg 360 ccagcctggc tttactaaca g 381 292 371 DNA Homo sapien misc_feature (1)...(371) n = A,T,C or G 292 gaaaaaataa tccgtttaat tgaaaaacct gnaggatact attccactcc cccanatgag 60 gaggctgagg anaccaaacc cctacatcac ctcgtagcca cttctgatac tcttcacgag 120 gcagcaggca aagacaattc ccaaaacctc nacaaaagca attccaaggg ctgctgcagc 180 taccaccanc acatttttcc tcagccagcc cccaatcttc tccacacagc cctccttatg 240 gatcgccttc tcgttgaaat taatcccaca gcccacagta acattaatgc ancaggagtc 300 ggggactcgg ttcttcgaca tggaagggat tttctcccaa tctgtgtagt tagcagcccc 360 acagcactta a 371 293 361 DNA Homo sapien misc_feature (1)...(361) n = A,T,C or G 293 gatttaaaag aaaacacttt attgttcagc aattaaaagt tagccaaata tgtatttttc 60 tccataattt attgngatgt tatcaacatc aagtaaaatg ctcattttca tcatttgctt 120 ctgttcatgt tttcttgaac acgtcttcaa ttttccttcc aaaatgctgc atgccacact 180 tgaggtaacg aagcanaagt atttttaaac atgacagcta anaacattca tctacagcaa 240 cctatatgct caatacatgc cgcgtgatcc tagtagtttt ttcacaacct tctacaagtt 300 tttggaaaac atctgttatg atgactttca tacaccttca cctcaaaggc tttcttgcac 360 c 361 294 391 DNA Homo sapien misc_feature (1)...(391) n = A,T,C or G 294 tattttaaag tttaattatg attcanaaaa aatcgagcga ataactttct ctgaaaaaat 60 atattgactc tgtatanacc acagttattg gggganaagg gctggtaggt taaattatcc 120 tattttttat tctgaaaatg atattaatan aaagtcccgt ttccagtctg attataaaga 180 tacatatgcc caaaatggct ganaataaat acaacaggaa atgcaaaagc tgtaaagcta 240 agggcatgca ananaaaatc tcanaatacc caaagnggca acaaggaacg tttggctgga 300 atttgaagtt atttcagtca tctttgtctt tggctccatg tttcaggatg cgtgtgaact 360 cgatgtaatt gaaattcccc tttttatcaa t 391 295 343 DNA Homo sapien misc_feature (1)...(343) n = A,T,C or G 295 ttcttttgtt ttattgataa cagaaactgt gcataattac agatttgatg aggaatctgc 60 aaataataaa gaatgtgtct actgccagca aaatacaatt attccatgcc ctctcaacat 120 acaaatatag agttcttcac accanatggc tctggtgtaa caaagccatt ttanatgttt 180 aattgtgctt ctacaaaacc ttcanagcat gaggtagttt cttttaccta cnatattttc 240 cacatttcca ttattacact tttagtgagc taaaatcctt ttaacatagc ctgcggatga 300 tctttcacaa aagccaagcc tcatttacaa agggtttatt tct 343 296 241 DNA Homo sapien misc_feature (1)...(241) n = A,T,C or G 296 ttcttggata ttggttgttt ttgtgaaaaa gtttttgttt ttcttctcag tcaactgaat 60 tatttctcta ctttgccctc ctgatgccca catgananaa cttaanataa tttctaacag 120 cttccacttt ggaaaaaaaa aaaacctgtt ttcctcatgg aaccccagga gttgaaagtg 180 gatanatcgc tctcaaaatc taaggctctg ttcagcttta cattatgtta cctgacgttt 240 t 241 297 391 DNA Homo sapien misc_feature (1)...(391) n = A,T,C or G 297 gttgtggctg anaatgctgg agatgctcag ttctctccct cacaaggtag gccacaaatt 60 cttggtggtg ccctcacatc tggggtcttc aggcaccagc catgcctgcc gaggagtgct 120 gtcaggacan accatgtccg tgctaggccc aggcacagcc caaccactcc tcatccaagt 180 ctctcccagg tttctggtcc cgatgggcaa ggatgacccc tccagtggct ggtaccccac 240 catcccacta cccctcacat gctctcactc tccatcaggt ccccaatcct ggcttccctc 300 ttcacgaact ctcaaagaaa aggaaggata aaacctaaat aaaccagaca gaagcagctc 360 tggaaaagta caaaaagaca gccagaggtg t 391 298 321 DNA Homo sapien misc_feature (1)...(321) n = A,T,C or G 298 caagccaaac tgtntccagc tttattaaan atactttcca taaacaatca tggtatttca 60 ggcaggacat gggcanacaa tcgttaacag tatacaacaa ctttcaaact cccttnttca 120 atggactacc aaaaatcaaa aagccactat aaaacccaat gaagtcttca tctgatgctc 180 tgaacaggga aagtttaaag ngagggttga catttcacat ttagcatgtt gtttaacaac 240 ttttcacaag ccgaccctga ctttcaggaa gtgaaatgaa aatggcanaa tttatctgaa 300 natccacaat ctaaaaatgg a 321 299 401 DNA Homo sapien misc_feature (1)...(401) n = A,T,C or G 299 tatcataaag agtgttgaag tttatttatt atagcaccat tgagacattt tgaaattgga 60 attggtaaaa aaataaaaca aaaagcattt gaattgtatt tggnggaaca gcaaaaaaag 120 agaagtatca tttttctttg tcaaattata ctgtttccaa acattttgga aataaataac 180 tggaattttg tcggtcactt gcactggttg acaagattag aacaagagga acacatatgg 240 agttaaattt tttttgttgg gatttcanat agagtttggt ttataaaaag caaacagggc 300 caacgtccac accaaattct tgatcaggac caccaatgtc atagggngca atatctacaa 360 taggtagtct cacagccttg cgtgttcgat attcaaagac t 401 300 188 DNA Homo sapien misc_feature (1)...(188) n = A,T,C or G 300 tgaatgcttt gtcatattaa gaaagttaaa gtgcaataat gtttgaanac aataagtggt 60 ggtgtatctt gtttctaata agataaactt ttttgtcttt gctttatctt attagggagt 120 tgtatgtcag tgtataaaac atactgtgtg gtataacagg cttaataaat tctttaaaag 180 gaaaaaaa 188 301 291 DNA Homo sapien 301 aagattttgt tttattttat tatggctaga aagacactgt tatagccaaa atcggcaatg 60 acactaaaga aatcctctgt gcttttcaat atgcaaatat atttcttcca agagttgccc 120 tggtgtgact tcaagagttc atgttaactt cttttctgga aacttccttt tcttagttgt 180 tgtattcttg aagagcctgg gccatgaaga gcttgcctaa gttttgggca gtgaactcct 240 tgatgttctg gcagtaagtg tttatctggc ctgcaatgag cagcgagtcc a 291 302 341 DNA Homo sapien misc_feature (1)...(341) n = A,T,C or G 302 tgatttttca taattttatt aaatnatcac tgggaaaact aatggttcgc gtatcacaca 60 attacactac aatctgatag gagtggtaaa accagccaat ggaatccagg taaagtacaa 120 aaacgccacc ttttattgtc ctgtcttatt tctcgggaag gagggttcta ctttacacat 180 ttcatgagcc agcagtggac ttgagttaca atgtgtaggt tccttgtggt tatagctgca 240 gaagaagcca tcaaattctt gaggacttga catctctcgg aaagaagcaa actagtggat 300 cccccgggct gcaggaattc gatatcaagc ttatcgatac c 341 303 361 DNA Homo sapien misc_feature (1)...(361) n = A,T,C or G 303 tgcagacagt aaatnaattt tatttgngtt cacagaacat actaggcgat ctcgacagtc 60 gctccgtgac agcccaccaa cccccaaccc tntacctcgc agccacccta aaggcgactt 120 caanaanatg gaaggatctc acggatctca ttcctaatgg tccgccgaag tctcacacag 180 tanacagacg gagttganat gctggaggat gcagtcacct cctaaactta cgacccacca 240 ccanacttca tcccagccgg gacgtcctcc cccacccgag tcctccccat ttcttctcct 300 actttgccgc agttccaggn gtcctgcttc caccagtccc acaaagctca ataaatacca 360 a 361 304 301 DNA Homo sapien misc_feature (1)...(301) n = A,T,C or G 304 ctctttacaa cagcctttat ttncggccct tgatcctgct cggatgctgg tggaggccct 60 tagctccgcc cgccaggctc tgtgccgcct ccccgcaggc gcanattcat gaacacggtg 120 ctcaggggct tgaggccgta ctcccccagc gggagctggt cctccagggg cttcccctcg 180 aaggtcagcc anaacaggtc gtcctgcaca ccctccagcc cgctcacttg ctgcttcagg 240 tgggccacgg tctgcgtcag ccgcacctcg taggtgctgc tgcggccctt gttattcctc 300 a 301 305 331 DNA Homo sapien misc_feature (1)...(331) n = A,T,C or G 305 ganaggctag taacatcagt tttattgggt tggggnggca accatagcct ggctgggggn 60 ggggctggcc ctcacaggtt gttgagttcc agcagggtct ggtccaaggt ctggtgaatc 120 tcgacgttct cctccttggc actggccaag gtctcttcta ggtcatcgat ggttttctcc 180 aactttgcca canacctctc ggcaaactct gctcgggtct cancctcctt cagcttctcc 240 tccaacagtt tgatctcctc ttcatattta tcttctttgg gggaatactc ctcctctgag 300 gccatcaggg acttgagggc ctggtccatg g 331 306 457 DNA Homo sapien 306 aatatgtaaa ggtaataact tttattatat taaagacaat gcaaacgaaa aacagaattg 60 agcagtgcaa aatttaaagg actgttttgt tctcaaagtt gcaagtttca aagccaaaag 120 aattatatgt atcaaatata taagtaaaaa aaagttagac tttcaagcct gtaatcccag 180 cactttggga ggctgaggca ggtggatcac taacattaaa aagacaacat tagattttgt 240 cgatttatag caattttata aatatataac tttgtcactt ggatcctgaa gcaaaataat 300 aaagtgaatt tgggattttt gtacttggta aaaagtttaa caccctaaat tcacaactag 360 tggatccccc gggctgcagg aattcgatat caagcttatc gataccgtcg acctcgaggg 420 ggggcccggt acccaattcg ccctatagtg agtcgta 457 307 491 DNA Homo sapien 307 gtgcttggac ggaacccggc gctcgttccc caccccggcc ggccgcccat agccagccct 60 ccgtcacctc ttcaccgcac cctcggactg ccccaaggcc cccgccgccg ctccagcgcc 120 gcgcagccac cgccgccgcc gccgcctctc cttagtcgcc gccatgacga ccgcgtccac 180 ctcgcaggtg cgccagaact accaccagga ctcagaggcc gccatcaacc gccagatcaa 240 cctggagctc tacgcctcct acgtttacct gtccatgtct tactactttg accgcgatga 300 tgtggctttg aagaactttg ccaaatactt tcttcaccaa tctcatgagg agagggaaca 360 tgctgagaaa ctgatgaagc tgcagaacca acgaggtggc cgaatcttcc ttcaggatat 420 caagaaacca gactgtgatg actgggagag cgggctgaat gcaatggagt gtgcattaca 480 tttggaaaaa a 491 308 421 DNA Homo sapien 308 ctcagcgctt cttctttctt ggtttgatcc tgactgctgt catggcgtgc cctctggaga 60 aggccctgga tgtgatggtg tccaccttcc acaagtactc gggcaaagag ggtgacaagt 120 tcaagctcaa caagtcagaa ctaaaggagc tgctgacccg ggagctgccc agcttcttgg 180 ggaaaaggac agatgaagct gctttccaga agctgatgag caacttggac agcaacaggg 240 acaacgaggt ggacttccaa gagtactgtg tcttcctgtc ctgcatcgcc atgatgtgta 300 acgaattctt tgaaggcttc ccagataagc agcccaggaa gaaatgaaaa ctcctctgat 360 gtggttgggg ggtctgccag ctggggccct ccctgtcgcc agtgggcact tttttttttc 420 c 421 309 321 DNA Homo sapien 309 accaaatggc ggatgacgcc ggtgcagcgg gggggcccgg gggccctggt ggccctggga 60 tggggaaccg cggtggcttc cgcggaggtt tcggcagtgg catccggggc cggggtcgcg 120 gccgtggacg gggccggggc cgaggccgcg gagctcgcgg aggcaaggcc gaggataagg 180 agtggatgcc cgtcaccaag ttgggccgct tggtcaagga catgaagatc aagtccctgg 240 aggagatcta tctcttctcc ctgcccatta aggaatcaga gatcattgat ttcttcctgg 300 gggcctctct caaggatgag g 321 310 381 DNA Homo sapien 310 ttaaccagcc atattggctc aataaatagc ttcggtaagg agttaatttc cttctagaaa 60 tcagtgccta tttttcctgg aaactcaatt ttaaatagtc caattccatc tgaagccaag 120 ctgttgtcat tttcattcgg tgacattctc tcccatgaca cccagaaggg gcagaagaac 180 cacatttttc atttatagat gtttgcatcc tttgtattaa aattattttg aaggggttgc 240 ctcattggat ggcttttttt tttttcctcc agggagaagg ggagaaatgt acttggaaat 300 taatgtatgt ttacatctct ttgcaaattc ctgtacatag agatatattt tttaagtgtg 360 aatgtaacaa catactgtga a 381 311 538 DNA Homo sapien 311 tttgaattta caccaagaac ttctcaataa aagaaaatca tgaatgctcc acaatttcaa 60 cataccacaa gagaagttaa tttcttaaca ttgtgttcta tgattatttg taagaccttc 120 accaagttct gatatctttt aaagacatag ttcaaaattg cttttgaaaa tctgtattct 180 tgaaaatatc cttgttgtgt attaggtttt taaataccag ctaaaggatt acctcactga 240 gtcatcagta ccctcctatt cagctcccca agatgatgtg tttttgctta ccctaagaga 300 ggttttcttc ttatttttag ataattcaag tgcttagata aattatgttt tctttaagtg 360 tttatggtaa actcttttaa agaaaattta atatgttata gctgaatctt tttggtaact 420 ttaaatcttt atcatagact ctgtacatat gttcaaatta gctgcttgcc tgatgtgtgt 480 atcatcggtg ggatgacaga acaaacatat ttatgatcat gaataatgtg ctttgtaa 538 312 176 DNA Homo sapien 312 ggaggagcag ctgagagata gggtcagtga atgcggttca gcctgctacc tctcctgtct 60 tcatagaacc attgccttag aattattgta tgacacgttt tttgttggtt aagctgtaag 120 gttttgttct ttgtgaacat gggtattttg aggggagggt ggagggagta gggaag 176 313 396 DNA Homo sapien 313 ccagcacccc caggccctgg gggacctggg ttctcagact gccaaagaag ccttgccatc 60 tggcgctccc atggctcttg caacatctcc ccttcgtttt tgagggggtc atgccggggg 120 agccaccagc ccctcactgg gttcggagga gagtcaggaa gggccaagca cgacaaagca 180 gaaacatcgg atttggggaa cgcgtgtcaa tcccttgtgc cgcagggctg ggcgggagag 240 actgttctgt tccttgtgta actgtgttgc tgaaagacta cctcgttctt gtcttgatgt 300 gtcaccgggg caactgcctg ggggcgggga tgggggcagg gtggaagcgg ctccccattt 360 tataccaaag gtgctacatc tatgtgatgg gtgggg 396 314 311 DNA Homo sapien 314 cctcaacatc ctcagagagg actggaagcc agtccttacg ataaactcca taatttatgg 60 cctgcagtat ctcttcttgg agcccaaccc cgaggaccca ctgaacaagg aggccgcaga 120 ggtcctgcag aacaaccggc ggctgtttga gcagaacgtg cagcgctcca tgcggggtgg 180 ctacatcggc tccacctact ttgagcgctg cctgaaatag ggttggcgca tacccacccc 240 cgccacggcc acaagccctg gcatcccctg caaatattta ttgggggcca tgggtagggg 300 tttggggggc g 311 315 336 DNA Homo sapien 315 tttagaacat ggttatcatc caagactact ctaccctgca acattgaact cccaagagca 60 aatccacatt cctcttgagt tctgcagctt ctgtgtaaat agggcagctg tcgtctatgc 120 cgtagaatca catgatctga ggaccattca tggaagctgc taaatagcct agtctgggga 180 gtcttccata aagttttgca tggagcaaac aaacaggatt aaactaggtt tggttccttc 240 agccctctaa aagcataggg cttagcctgc aggcttcctt gggctttctc tgtgtgtgta 300 gttttgtaaa cactatagca tctgttaaga tccagt 336 316 436 DNA Homo sapien 316 aacatggtct gcgtgcctta agagagacgc ttcctgcaga acaggacctg actacaaaga 60 atgtttccat tggaattgtt ggtaaagact tggagtttac aatctatgat gatgatgatg 120 tgtctccatt cctggaaggt cttgaagaaa gaccacagag aaaggcacag cctgctcaac 180 ctgctgatga acctgcagaa aaggctgatg aaccaatgga acattaagtg ataagccagt 240 ctatatatgt attatcaaat atgtaagaat acaggcacca catactgatg acaataatct 300 atactttgaa ccaaaagttg cagagtggtg gaatgctatg ttttaggaat cagtccagat 360 gtgagttttt tccaagcaac ctcactgaaa cctatataat ggaatacatt tttctttgaa 420 agggtctgta taatca 436 317 196 DNA Homo sapien 317 tattccttgt gaagatgata tactattttt gttaagcgtg tctgtattta tgtgtgagga 60 gctgctggct tgcagtgcgc gtgcacgtgg agagctggtg cccggagatt ggacggcctg 120 atgctccctc ccctgccctg gtccagggaa gctggccgag ggtcctggct cctgaggggc 180 atctgcccct ccccca 196 318 381 DNA Homo sapien misc_feature (1)...(381) n = A,T,C or G 318 gacgcttnng ccgtaacgat gatcggagac atcctgctgt tcgggacgtt gctgatgaat 60 gccggggcgg tgctgaactt taagctgaaa aagaaggaca cncagggctt tggggaggag 120 tncagggagc ccaacacagg tgacaacatc cgggaattct tgctgancct cagatacttt 180 cnaatcttca tcnccctgtg gaacatcttc atgatgttct gcatgattgt gctgntcggc 240 tcttgaatcc cancgatgaa accannaact cactttcccg ggatgccgan tctccattcc 300 tccattcctg atgacttcaa naatgttttt gaccaaaaaa ccgacaacct tcccagaaag 360 tccaagctcg tggtgggngg a 381 319 506 DNA Homo sapien 319 ctaagcttta cgaatggggt gacaacttat gataaaaact agagctagtg aattagccta 60 tttgtaaata cctttgttat aattgatagg atacatcttg gacatggaat tgttaagcca 120 cctctgagca gtgtatgtca ggacttgttc attaggttgg cagcagaggg gcagaaggaa 180 ttatacaggt agagatgtat gcagatgtgt ccatatatgt ccatatttac attttgatag 240 ccattgatgt atgcatctct tggctgtact ataagaacac attaattcaa tggaaataca 300 ctttgctaat attttaatgg tatagatctg ctaatgaatt ctcttaaaaa catactgtat 360 tctgttgctg tgtgtttcat tttaaattga gcattaaggg aatgcagcat ttaaatcaga 420 actctgccaa tgcttttatc tagaggcgtg ttgccatttt tgtcttatat gaaatttctg 480 tcccaagaaa ggcaggatta catctt 506 320 351 DNA Homo sapien 320 ctgacctgca ggacgaaacc atgaagagcc tgatccttct tgccatcctg gccgccttag 60 cggtagtaac tttgtgttat gaatcacatg aaagcatgga atcttatgaa cttaatccct 120 tcattaacag gagaaatgca aataccttca tatcccctca gcagagatgg agagctaaag 180 tccaagagag gatccgagaa cgctctaagc ctgtccacga gctcaatagg gaagcctgtg 240 atgactacag actttgcgaa cgctacgcca tggtttatgg atacaatgct gcctataatc 300 gctacttcag gaagcgccga gggaccaaat gagactgagg gaagaaaaaa a 351 321 421 DNA Homo sapien 321 ctcggaggcg ttcagctgct tcaagatgaa gctgaacatc tccttcccag ccactggctg 60 ccagaaactc attgaagtgg acgatgaacg caaacttcgt actttctatg agaagcgtat 120 ggccacagaa gttgctgctg acgctctggg tgaagaatgg aagggttatg tggtccgaat 180 cagtggtggg aacgacaaac aaggtttccc catgaagcag ggtgtcttga cccatggccg 240 tgtccgcctg ctactgagta aggggcattc ctgttacaga ccaaggagaa ctggagaaag 300 aaagagaaaa tcagttcgtg gttgcattgt ggatgcaaat ctgagcgttc tcaacttggt 360 tattgtaaaa aaaggagaga aggatattcc tggactgact gatactacag tgcctcgccg 420 c 421 322 521 DNA Homo sapien 322 agcagctctc ctgccacagc tcctcacccc ctgaaaatgt tcgcctgctc caagtttgtc 60 tccactccct ccttggtcaa gagcacctca cagctgctga gccgtccgct atctgcagtg 120 gtgctgaaac gaccggagat actgacagat gagagcctca gcagcttggc agtctcatgt 180 ccccttacct cacttgtctc tagccgcagc ttccaaacca gcgccatttc aagggacatc 240 gacacagcag ccaagttcat tggagctggg gctgccacag ttggggtggc tggttctggg 300 gctgggattg gaactgtgtt tgggagcctc atcattggtt atgccaggaa cccttctctg 360 aagcaacagc tcttctccta cgccattctg ggctttgccc tctcggaggc catggggctc 420 ttttgtctga tggtagcctt tctcatcctc tttgccatgt gaaggagccg tctccacctc 480 ccatagttct cccgcgtctg gttggccccg tgtgttcctt t 521 323 435 DNA Homo sapien 323 ccgaggtcgc acgcgtgaga cttctccgcc gcagacgccg ccgcgatgcg ctacgtcgcc 60 tcctacctgc tggctgccct agggggcaac tcctccccca gcgccaagga catcaagaag 120 atcttggaca gcgtgggtat cgaggcggac gacgaccggc tcaacaaggt tatcagtgag 180 ctgaatggaa aaaacattga agacgtcatt gcccagggta ttggcaagct tgccagtgta 240 cctgctggtg gggctgtagc cgtctctgct gccccaggct ctgcagcccc tgctgctggt 300 tctgcccctg ctgcagcaga ggagaagaaa gatgagaaga aggaggagtc tgaagagtca 360 gatgatgaca tgggatttgg cctttttgat taaattcctg ctcccctgca aataaagcct 420 ttttacacat ctcaa 435 324 521 DNA Homo sapien 324 aggagatcga ctttcggtgc ccgcaagacc agggctggaa cgccgagatc acgctgcaga 60 tggtgcagta caagaatcgt caggccatcc tggcggtcaa atccacgcgg cagaagcagc 120 agcacctggt ccagcagcag cccccctcgc agccgcagcc gcagccgcag ctccagcccc 180 aaccccagcc tcagcctcag ccgcaacccc agccccaatc acaaccccag cctcagcccc 240 aacccaagcc tcagccccag cagctccacc cgtatccgca tccacatcca catccacact 300 ctcatcctca ctcgcaccca caccctcacc cgcacccgca tccgcaccaa ataccgcacc 360 cacacccaca gccgcactcg cagccgcacg ggcaccggct tctccgcagc acctccaact 420 ctgcctgaaa ggggcagctc ccgggcaaga caaggttttg aggacttgag gaagtgggac 480 gagcacattt ctattgtctt cacttggatc aaaagcaaaa c 521 325 451 DNA Homo sapien 325 attttcattt ccattaacct ggaagctttc atgaatattc tcttctttta aaacatttta 60 acattattta aacagaaaaa gatgggctct ttctggttag ttgttacatg atagcagaga 120 tatttttact tagattactt tgggaatgag agattgttgt cttgaactct ggcactgtac 180 agtgaatgtg tctgtagttg tgttagtttg cattaagcat gtataacatt caagtatgtc 240 atccaaataa gaggcatata cattgaattg tttttaatcc tctgacaagt tgactcttcg 300 acccccaccc ccacccaaga cattttaata gtaaatagag agagagagaa gagttaatga 360 acatgaggta gtgttccact ggcaggatga cttttcaata gctcaaatca atttcagtgc 420 ctttatcact tgaattatta acttaatttg a 451 326 421 DNA Homo sapien misc_feature (1)...(421) n = A,T,C or G 326 cgcggtcgta agggctgagg atttttggtc cgcacgctcc tgctcctgac tcaccgctgt 60 tcgctctcgc cgaggaacaa gtcggtcagg aagcccgcgc gcaacagcca tggcttttaa 120 ggataccgga aaaacacccg tggagccgga ggtggcaatt caccgaattc gaatcaccct 180 aacaagccgc aacgtaaaat ccttggaaaa ggtgtgtgct gacttgataa gaggcgcaaa 240 agaaaagaat ctcaaagtga aaggaccagt tcgaatgcct accaagactt tgagantcac 300 tacaagaaaa actccttgtg gtgaaggttc taagacgtgg gatcgtttcc agatgagaat 360 tcacaagcga ctcattgact tgcacagtcc ttctgagatt gttaagcaga ttacttccat 420 c 421 327 456 DNA Homo sapien 327 atcttgacga ggctgcggtg tctgctgcta ttctccgagc ttcgcaatgc cgcctaagga 60 cgacaagaag aagaaggacg ctggaaagtc ggccaagaaa gacaaagacc cagtgaacaa 120 atccgggggc aaggccaaaa agaagaagtg gtccaaaggc aaagttcggg acaagctcaa 180 taacttagtc ttgtttgaca aagctaccta tgataaactc tgtaaggaag ttcccaacta 240 taaacttata accccagctg tggtctctga gagactgaag attcgaggct ccctggccag 300 ggcagccctt caggagctcc ttagtaaagg acttatcaaa ctggtttcaa agcacagagc 360 tcaagtaatt tacaccagaa ataccaaggg tggagatgct ccagctgctg gtgaagatgc 420 atgaataggt ccaaccagct gtacatttgg aaaaat 456 328 471 DNA Homo sapien 328 gtggaagtga catcgtcttt aaaccctgcg tggcaatccc tgacgcaccg ccgtgatgcc 60 cagggaagac agggcgacct ggaagtccaa ctacttcctt aagatcatcc aactattgga 120 tgattatccg aaatgtttca ttgtgggagc agacaatgtg ggctccaagc agatgcagca 180 gatccgcatg tcccttcgcg ggaaggctgt ggtgctgatg ggcaagaaca ccatgatgcg 240 caaggccatc cgagggcacc tggaaaacaa cccagctctg gagaaactgc tgcctcatat 300 ccgggggaat gtgggctttg tgttcaccaa ggaggacctc actgagatca gggacatgtt 360 gctggccaat aaggtgccag ctgctgcccg tgctggtgcc attgccccat gtgaagtcac 420 tgtgccagcc cagaacactg gtctcgggcc cgagaagacc tcctttttcc a 471 329 278 DNA Homo sapien misc_feature (1)...(278) n = A,T,C or G 329 gtttaaactt aagcttggta ccgagctcgg atccactagt ccagtgtggt ggaattctag 60 aaattgagat gcccccccag gccagcaaat gttccttttt gttcaaagtc tatttttatt 120 ccttgatatt tttctttttt tttttttttt ttgnggatgg ggacttgtga atttttctaa 180 aggtgctatt taacatggga gganagcgtg tgcggctcca gcccagcccg ctgctcactt 240 tccaccctct ctccacctgc ctctggcttc tcaggcct 278 330 338 DNA Homo sapien 330 ctcaggcttc aacatcgaat acgccgcagg ccccttcgcc ctattcttca tagccgaata 60 cacaaacatt attataataa acaccctcac cactacaatc ttcctaggaa caacatatga 120 cgcactctcc cctgaactct acacaacata ttttgtcacc aagaccctac ttctaacctc 180 cctgttctta tgaattcgaa cagcataccc ccgattccgc tacgaccaac tcatacacct 240 cctatgaaaa aacttcctac cactcaccct agcattactt atatgatatg tctccatacc 300 cattacaatc tccagcattc cccctcaaac ctaaaaaa 338 331 2820 DNA Homo sapiens 331 tggcaaaatc ctggagccag aagaaaggac agcagcattg atcaatctta cagctaacat 60 gttgtacctg gaaaacaatg cccagactca atttagtgag ccacagtaca cgaacctggg 120 gctcctgaac agcatggacc agcagattcg gaacggctcc tcgtccacca gtccctataa 180 cacagaccac gcgcagaaca gcgtcacggc gccctcgccc tacgcacagc ccagccccac 240 cttcgatgct ctctctccat cacccgccat cccctccaac accgactacc caggcccgca 300 cagttccgac gtgtccttcc agcagtcgag caccgccaag tcggccacct ggacgtattc 360 cactgaactg aagaaactct actgccaaat tgcaaagaca tgccccatcc agatcaaggt 420 gatgacccca cctcctcagg gagctgttat ccgcgccatg cctgtctaca aaaaagctga 480 gcacgtcacg gaggtggtga agcggtgccc caaccatgag ctgagccgtg agttcaacga 540 gggacagatt gcccctccta gtcatttgat tcgagtagag gggaacagcc atgcccagta 600 tgtagaagat cccatcacag gaagacagag tgtgctggta ccttatgagc caccccaggt 660 tggcactgaa ttcacgacag tcttgtacaa tttcatgtgt aacagcagtt gtgttggagg 720 gatgaaccgc cgtccaattt taatcattgt tactctggaa accagagatg ggcaagtcct 780 gggccgacgc tgctttgagg cccggatctg tgcttgccca ggaagagaca ggaaggcgga 840 tgaagatagc atcagaaagc agcaagtttc ggacagtaca aagaacggtg atggtacgaa 900 gcgcccgttt cgtcagaaca cacatggtat ccagatgaca tccatcaaga aacgaagatc 960 cccagatgat gaactgttat acttaccagt gaggggccgt gagacttatg aaatgctgtt 1020 gaagatcaaa gagtccctgg aactcatgca gtaccttcct cagcacacaa ttgaaacgta 1080 caggcaacag caacagcagc agcaccagca cttacttcag aaacagacct caatacagtc 1140 tccatcttca tatggtaaca gctccccacc tctgaacaaa atgaacagca tgaacaagct 1200 gccttctgtg agccagctta tcaaccctca gcagcgcaac gccctcactc ctacaaccat 1260 tcctgatggc atgggagcca acattcccat gatgggcacc cacatgccaa tggctggaga 1320 catgaatgga ctcagcccca cccaggcact ccctccccca ctctccatgc catccacctc 1380 ccactgcaca cccccacctc cgtatcccac agattgcagc attgtcagtt tcttagcgag 1440 gttgggctgt tcatcatgtc tggactattt cacgacccag gggctgacca ccatctatca 1500 gattgagcat tactccatgg atgatctggc aagtctgaaa atccctgagc aatttcgaca 1560 tgcgatctgg aagggcatcc tggaccaccg gcagctccac gaattctcct ccccttctca 1620 tctcctgcgg accccaagca gtgcctctac agtcagtgtg ggctccagtg agacccgggg 1680 tgagcgtgtt attgatgctg tgcgattcac cctccgccag accatctctt tcccaccccg 1740 agatgagtgg aatgacttca actttgacat ggatgctcgc cgcaataagc aacagcgcat 1800 caaagaggag ggggagtgag cctcaccatg tgagctcttc ctatccctct cctaactgcc 1860 agccccctaa aagcactcct gcttaatctt caaagccttc tccctagctc ctccccttcc 1920 tcttgtctga tttcttaggg gaaggagaag taagaggcta cctcttacct aacatctgac 1980 ctggcatcta attctgattc tggctttaag ccttcaaaac tatagcttgc agaactgtag 2040 ctgccatggc taggtagaag tgagcaaaaa agagttgggt gtctccttaa gctgcagaga 2100 tttctcattg acttttataa agcatgttca cccttatagt ctaagactat atatataaat 2160 gtataaatat acagtataga tttttgggtg gggggcattg agtattgttt aaaatgtaat 2220 ttaaatgaaa gaaaattgag ttgcacttat tgaccatttt ttaatttact tgttttggat 2280 ggcttgtcta tactccttcc cttaaggggt atcatgtatg gtgataggta tctagagctt 2340 aatgctacat gtgagtgcga tgatgtacag attctttcag ttctttggat tctaaataca 2400 tgccacatca aacctttgag tagatccatt tccattgctt attatgtagg taagactgta 2460 gatatgtatt cttttctcag tgttggtata ttttatatta ctgacatttc ttctagtgat 2520 gatggttcac gttggggtga tttaatccag ttataagaag aagttcatgt ccaaacggtc 2580 ctctttagtt tttggttggg aatgaggaaa attcttaaaa ggcccatagc agccagttca 2640 aaaacacccg acgtcatgta tttgagcata tcagtaaccc ccttaaattt aatacccaga 2700 taccttatct tacaatgttg attgggaaaa catttgctgc ccattacaga ggtattaaaa 2760 ctaaatttca ctactagatt gactaactca aatacacatt tgctactgtt gtaagaattc 2820 332 2270 DNA Homo sapiens 332 tcgttgatat caaagacagt tgaaggaaat gaattttgaa acttcacggt gtgccaccct 60 acagtactgc cctgaccctt acatccagcg tttcgtagaa acccagctca tttctcttgg 120 aaagaaagtt attaccgatc caccatgtcc cagagcacac agacaaatga attcctcagt 180 ccagaggttt tccagcatat ctgggatttt ctggaacagc ctatatgttc agttcagccc 240 attgacttga actttgtgga tgaaccatca gaagatggtg cgacaaacaa gattgagatt 300 agcatggact gtatccgcat gcaggactcg gacctgagtg accccatgtg gccacagtac 360 acgaacctgg ggctcctgaa cagcatggac cagcagattc agaacggctc ctcgtccacc 420 agtccctata acacagacca cgcgcagaac agcgtcacgg cgccctcgcc ctacgcacag 480 cccagctcca ccttcgatgc tctctctcca tcacccgcca tcccctccaa caccgactac 540 ccaggcccgc acagtttcga cgtgtccttc cagcagtcga gcaccgccaa gtcggccacc 600 tggacgtatt ccactgaact gaagaaactc tactgccaaa ttgcaaagac atgccccatc 660 cagatcaagg tgatgacccc acctcctcag ggagctgtta tccgcgccat gcctgtctac 720 aaaaaagctg agcacgtcac ggaggtggtg aagcggtgcc ccaaccatga gctgagccgt 780 gaattcaacg agggacagat tgcccctcct agtcatttga ttcgagtaga ggggaacagc 840 catgcccagt atgtagaaga tcccatcaca ggaagacaga gtgtgctggt accttatgag 900 ccaccccagg ttggcactga attcacgaca gtcttgtaca atttcatgtg taacagcagt 960 tgtgttggag ggatgaaccg ccgtccaatt ttaatcattg ttactctgga aaccagagat 1020 gggcaagtcc tgggccgacg ctgctttgag gcccggatct gtgcttgccc aggaagagac 1080 aggaaggcgg atgaagatag catcagaaag cagcaagttt cggacagtac aaagaacggt 1140 gatggtacga agcgcccgtt tcgtcagaac acacatggta tccagatgac atccatcaag 1200 aaacgaagat ccccagatga tgaactgtta tacttaccag tgaggggccg tgagacttat 1260 gaaatgctgt tgaagatcaa agagtccctg gaactcatgc agtaccttcc tcagcacaca 1320 attgaaacgt acaggcaaca gcaacagcag cagcaccagc acttacttca gaaacagacc 1380 tcaatacagt ctccatcttc atatggtaac agctccccac ctctgaacaa aatgaacagc 1440 atgaacaagc tgccttctgt gagccagctt atcaaccctc agcagcgcaa cgccctcact 1500 cctacaacca ttcctgatgg catgggagcc aacattccca tgatgggcac ccacatgcca 1560 atggctggag acatgaatgg actcagcccc acccaggcac tccctccccc actctccatg 1620 ccatccacct cccactgcac acccccacct ccgtatccaa cagattgcag cattgtcggt 1680 ttcttagcga ggttgggctg ttcatcatgt ctggactatt tcacgaccca ggggctgacc 1740 accatctatc agattgagca ttactccatg gatgatctgg caagtctgaa aatccctgag 1800 caatttcgac atgcgatctg gaagggcatc ctggaccacc ggcagctcca cgaattctcc 1860 tccccttctc atctcctgcg gaccccaagc agtgcctcta cagtcagtgt gggctccagt 1920 gagacccggg gtgagcgtgt tattgatgct gtgcgattca ccctccgcca gaccatctct 1980 ttcccacccc gagatgagtg gaatgacttc aactttgaca tggatgctcg ccgcaataag 2040 caacagcgca tcaaagagga gggggagtga gcctcaccat gtgagctctt cctatccctc 2100 tcctaactgc cagcccccta aaagcactcc tgcttaatct tcaaagcctt ctccctagct 2160 cctccccttc ctcttgtctg atttcttagg ggaaggagaa gtaagaggct acctcttacc 2220 taacatctga cctggcatct aattctgatt ctggctttaa gccttcaaaa 2270 333 2816 DNA Homo sapiens 333 tcgttgatat caaagacagt tgaaggaaat gaattttgaa acttcacggt gtgccaccct 60 acagtactgc cctgaccctt acatccagcg tttcgtagaa acccagctca tttctcttgg 120 aaagaaagtt attaccgatc caccatgtcc cagagcacac agacaaatga attcctcagt 180 ccagaggttt tccagcatat ctgggatttt ctggaacagc ctatatgttc agttcagccc 240 attgacttga actttgtgga tgaaccatca gaagatggtg cgacaaacaa gattgagatt 300 agcatggact gtatccgcat gcaggactcg gacctgagtg accccatgtg gccacagtac 360 acgaacctgg ggctcctgaa cagcatggac cagcagattc agaacggctc ctcgtccacc 420 agtccctata acacagacca cgcgcagaac agcgtcacgg cgccctcgcc ctacgcacag 480 cccagctcca ccttcgatgc tctctctcca tcacccgcca tcccctccaa caccgactac 540 ccaggcccgc acagtttcga cgtgtccttc cagcagtcga gcaccgccaa gtcggccacc 600 tggacgtatt ccactgaact gaagaaactc tactgccaaa ttgcaaagac atgccccatc 660 cagatcaagg tgatgacccc acctcctcag ggagctgtta tccgcgccat gcctgtctac 720 aaaaaagctg agcacgtcac ggaggtggtg aagcggtgcc ccaaccatga gctgagccgt 780 gaattcaacg agggacagat tgcccctcct agtcatttga ttcgagtaga ggggaacagc 840 catgcccagt atgtagaaga tcccatcaca ggaagacaga gtgtgctggt accttatgag 900 ccaccccagg ttggcactga attcacgaca gtcttgtaca atttcatgtg taacagcagt 960 tgtgttggag ggatgaaccg ccgtccaatt ttaatcattg ttactctgga aaccagagat 1020 gggcaagtcc tgggccgacg ctgctttgag gcccggatct gtgcttgccc aggaagagac 1080 aggaaggcgg atgaagatag catcagaaag cagcaagttt cggacagtac aaagaacggt 1140 gatggtacga agcgcccgtt tcgtcagaac acacatggta tccagatgac atccatcaag 1200 aaacgaagat ccccagatga tgaactgtta tacttaccag tgaggggccg tgagacttat 1260 gaaatgctgt tgaagatcaa agagtccctg gaactcatgc agtaccttcc tcagcacaca 1320 attgaaacgt acaggcaaca gcaacagcag cagcaccagc acttacttca gaaacatctc 1380 ctttcagcct gcttcaggaa tgagcttgtg gagccccgga gagaaactcc aaaacaatct 1440 gacgtcttct ttagacattc caagccccca aaccgatcag tgtacccata gagccctatc 1500 tctatatttt aagtgtgtgt gttgtatttc catgtgtata tgtgagtgtg tgtgtgtgta 1560 tgtgtgtgcg tgtgtatcta gccctcataa acaggacttg aagacacttt ggctcagaga 1620 cccaactgct caaaggcaca aagccactag tgagagaatc ttttgaaggg actcaaacct 1680 ttacaagaaa ggatgttttc tgcagatttt gtatccttag accggccatt ggtgggtgag 1740 gaaccactgt gtttgtctgt gagctttctg ttgtttcctg ggagggaggg gtcaggtggg 1800 gaaaggggca ttaagatgtt tattggaacc cttttctgtc ttcttctgtt gtttttctaa 1860 aattcacagg gaagcttttg agcaggtctc aaacttaaga tgtcttttta agaaaaggag 1920 aaaaaagttg ttattgtctg tgcataagta agttgtaggt gactgagaga ctcagtcaga 1980 cccttttaat gctggtcatg taataatatt gcaagtagta agaaacgaag gtgtcaagtg 2040 tactgctggg cagcgaggtg atcattacca aaagtaatca actttgtggg tggagagttc 2100 tttgtgagaa cttgcattat ttgtgtcctc ccctcatgtg taggtagaac atttcttaat 2160 gctgtgtacc tgcctctgcc actgtatgtt ggcatctgtt atgctaaagt ttttcttgta 2220 catgaaaccc tggaagacct actacaaaaa aactgttgtt tggcccccat agcaggtgaa 2280 ctcattttgt gcttttaata gaaagacaaa tccaccccag taatattgcc cttacgtagt 2340 tgtttaccat tattcaaagc tcaaaataga atttgaagcc ctctcacaaa atctgtgatt 2400 aatttgctta attagagctt ctatccctca agcctaccta ccataaaacc agccatatta 2460 ctgatactgt tcagtgcatt tagccaggag acttacgttt tgagtaagtg agatccaagc 2520 agacgtgtta aaatcagcac tcctggactg gaaattaaag attgaaaggg tagactactt 2580 ttcttttttt tactcaaaag tttagagaat ctctgtttct ttccatttta aaaacatatt 2640 ttaagataat agcataaaga ctttaaaaat gttcctcccc tccatcttcc cacacccagt 2700 caccagcact gtattttctg tcaccaagac aatgatttct tgttattgag gctgttgctt 2760 ttgtggatgt gtgattttaa ttttcaataa acttttgcat cttggtttaa aagaaa 2816 334 2082 DNA Homo sapiens 334 agatgctaca gcgactgcac acccaggctg tatgatacag cctattgctc ccgggctgca 60 aacctgtcca gcatgtgatg tggtgggata ctgaattgaa taccgaatac tgtaggcaat 120 tgtaacacag tggtaagtct ttgtgtatct aaacatagct aaacaccaaa aggtatagta 180 agaatatggt attataatct tatggaacta tcattgtata tgtggtttgt caaccagaat 240 gtagttatac agcacaggac tgtgcttatg atgtgccaag cacagctctc agtactaact 300 cctttaatct tcatatcaac cctaggaggt aacttcttaa gtagattcat attgtaaggg 360 tctcggggtg ggggggttgg caaaatcctg gagccagaag aaaggacagc agcattgatc 420 aatcttacag ctaacatgtt gtacctggaa aacaatgccc agactcaatt tagtgagcca 480 cagtacacga acctggggct cctgaacagc atggaccagc agattcagaa cggctcctcg 540 tccaccagtc cctataacac agaccacgcg cagaacagcg tcacggcgcc ctcgccctac 600 gcacagccca gctccacctt cgatgctctc tctccatcac ccgccatccc ctccaacacc 660 gactacccag gcccgcacag tttcgacgtg tccttccagc agtcgagcac cgccaagtcg 720 gccacctgga cgtattccac tgaactgaag aaactctact gccaaattgc aaagacatgc 780 cccatccaga tcaaggtgat gaccccacct cctcagggag ctgttatccg cgccatgcct 840 gtctacaaaa aagctgagca cgtcacggag gtggtgaagc ggtgccccaa ccatgagctg 900 agccgtgaat tcaacgaggg acagattgcc cctcctagtc atttgattcg agtagagggg 960 aacagccatg cccagtatgt agaagatccc atcacaggaa gacagagtgt gctggtacct 1020 tatgagccac cccaggttgg cactgaattc acgacagtct tgtacaattt catgtgtaac 1080 agcagttgtg ttggagggat gaaccgccgt ccaattttaa tcattgttac tctggaaacc 1140 agagatgggc aagtcctggg ccgacgctgc tttgaggccc ggatctgtgc ttgcccagga 1200 agagacagga aggcggatga agatagcatc agaaagcagc aagtttcgga cagtacaaag 1260 aacggtgatg gtacgaagcg cccgtctcgt cagaacacac atggtatcca gatgacatcc 1320 atcaagaaac gaagatcccc agatgatgaa ctgttatact taccagtgag gggccgtgag 1380 acttatgaaa tgctgttgaa gatcaaagag tccctggaac tcatgcagta ccttcctcag 1440 cacacaattg aaacgtacag gcaacagcaa cagcagcagc accagcactt acttcagaaa 1500 cagtgagtgt atcaacgtgt cattttagga ggcatgagtg acggtgactt tatttggatc 1560 agcaataggg tgattgatga gcaatgtgga acataatggg agatagcaga ttgtcataga 1620 ttcagatgac ctggtatggc aaccctcttt cagttgcaac cttttttacg tgtcttatta 1680 taaccttccc ttcagaattc cacttatgtt ctgaaattaa atacaaacca tttctggtga 1740 attacaaaga aactcacact aacagttctc ttctctatat gcctggtcca tacacactaa 1800 cagtaagtac acactctatt tggtagtgat gtgtatattt gaaaacatga aatcttttct 1860 catcccaatg gattgtctta taaatctcct gggatgcaca ctatccactt ttgggaataa 1920 cactgtagac cagggatagc aaataggctt tactataata taaagtgact tgtttgaatg 1980 ctgtaatgag aagaattctg agacctagtg catgataatt ggggaaatat ctgggtgcag 2040 aaggataagg tagcatcatg ttgccgtatt ttagcatctc tg 2082 335 4849 DNA Homo sapiens 335 cgttgatatc aaagacagtt gaaggaaatg aattttgaaa cttcacggtg tgccacccta 60 cagtactgcc ctgaccctta catccagcgt ttcgtagaaa ccccagctca tttctcttgg 120 aaagaaagtt attaccgatc caccatgtcc cagagcacac agacaaatga attcctcagt 180 ccagaggttt tccagcatat ctgggatttt ctggaacagc ctatatgttc agttcagccc 240 attgacttga actttgtgga tgaaccatca gaagatggtg cgacaaacaa gattgagatt 300 agcatggact gtatccgcat gcaggactcg gacctgagtg accccatgtg gccacagtac 360 acgaacctgg ggctcctgaa cagcatggac cagcagattc agaacggctc ctcgtccacc 420 agtccctata acacagacca cgcgcagaac agcgtcacgg cgccctcgcc ctacgcacag 480 cccagctcca ccttcgatgc tctctctcca tcacccgcca tcccctccaa caccgactac 540 ccaggcccgc acagtttcga cgtgtccttc cagcagtcga gcaccgccaa gtcggccacc 600 tggacgtatt ccactgaact gaagaaactc tactgccaaa ttgcaaagac atgccccatc 660 cagatcaagg tgatgacccc acctcctcag ggagctgtta tccgcgccat gcctgtctac 720 aaaaaagctg agcacgtcac ggaggtggtg aagcggtgcc ccaaccatga gctgagccgt 780 gaattcaacg agggacagat tgcccctcct agtcatttga ttcgagtaga ggggaacagc 840 catgcccagt atgtagaaga tcccatcaca ggaagacaga gtgtgctggt accttatgag 900 ccaccccagg ttggcactga attcacgaca gtcttgtaca atttcatgtg taacagcagt 960 tgtgttggag ggatgaaccg ccgtccaatt ttaatcattg ttactctgga aaccagagat 1020 gggcaagtcc tgggccgacg ctgctttgag gcccggatct gtgcttgccc aggaagagac 1080 aggaaggcgg atgaagatag catcagaaag cagcaagttt cggacagtac aaagaacggt 1140 gatggtacga agcgcccgtt tcgtcagaac acacatggta tccagatgac atccatcaag 1200 aaacgaagat ccccagatga tgaactgtta tacttaccag tgaggggccg tgagacttat 1260 gaaatgctgt tgaagatcaa agagtccctg gaactcatgc agtaccttcc tcagcacaca 1320 attgaaacgt acaggcaaca gcaacagcag cagcaccagc acttacttca gaaacagacc 1380 tcaatacagt ctccatcttc atatggtaac agctccccac ctctgaacaa aatgaacagc 1440 atgaacaagc tgccttctgt gagccagctt atcaaccctc agcagcgcaa cgccctcact 1500 cctacaacca ttcctgatgg catgggagcc aacattccca tgatgggcac ccacatgcca 1560 atggctggag acatgaatgg actcagcccc acccaggcac tccctccccc actctccatg 1620 ccatccacct cccagtgcac acccccacct ccgtatccca cagattgcag cattgtcagt 1680 ttcttagcga ggttgggctg ttcatcatgt ctggactatt tcacgaccca ggggctgacc 1740 accatctatc agattgagca ttactccatg gatgatctgg caagtctgaa aatccctgag 1800 caatttcgac atgcgatctg gaagggcatc ctggaccacc ggcagctcca cgaattctcc 1860 tccccttctc atctcctgcg gaccccaagc agtgcctcta cagtcagtgt gggctccagt 1920 gagacccggg gtgagcgtgt tattgatgct gtgcgattca ccctccgcca gaccatctct 1980 ttcccacccc gagatgagtg gaatgacttc aactttgaca tggatgctcg ccgcaataag 2040 caacagcgca tcaaagagga gggggagtga gcctcaccat gtgagctctt cctatccctc 2100 tcctaactgc cagcycccta aaagcactcc tgcttaatct tcaaagcctt ctccctagct 2160 cctccccttc ctcttgtctg atttcttagg ggaaggagaa gtaagaggct acctcttacc 2220 taacatctga cctggcatct aattctgatt ctggctttaa gccttcaaaa ctatagcttg 2280 cagaactgta gctgccatgg ctaggtagaa gtgagcaaaa aagagttggg tgtctcctta 2340 agctgcagag atttctcatt gacttttata aagcatgttc acccttatag tctaagacta 2400 tatatataaa tgtataaata tacagtatag atttttgggt ggggggcatt gagtattgtt 2460 taaaatgtaa tttaaatgaa agaaaattga gttgcactta ttgaccattt tttaatttac 2520 ttgttttgga tggcttgtct atactccttc ccttaagggg tatcatgtat ggtgataggt 2580 atctagagct taatgctaca tgtgagtgac gatgatgtac agattctttc agttctttgg 2640 attctaaata catgccacat caaacctttg agtagatcca tttccattgc ttattatgta 2700 ggtaagactg tagatatgta ttcttttctc agtgttggta tattttatat tactgacatt 2760 tcttctagtg atgatggttc acgttggggt gatttaatcc agttataaga agaagttcat 2820 gtccaaacgt cctctttagt ttttggttgg gaatgaggaa aattcttaaa aggcccatag 2880 cagccagttc aaaaacaccc gacgtcatgt atttgagcat atcagtaacc cccttaaatt 2940 taataccaga taccttatct tacaatattg attgggaaaa catttgctgc cattacagag 3000 gtattaaaac taaatttcac tactagattg actaactcaa atacacattt gctactgttg 3060 taagaattct gattgatttg attgggatga atgccatcta tctagttcta acagtgaagt 3120 tttactgtct attaatattc agggtaaata ggaatcattc agaaatgttg agtctgtact 3180 aaacagtaag atatctcaat gaaccataaa ttcaactttg taaaaatctt ttgaagcata 3240 gataatattg tttggtaaat gtttcttttg tttggtaaat gtttctttta aagaccctcc 3300 tattctataa aactctgcat gtagaggctt gtttaccttt ctctctctaa ggtttacaat 3360 aggagtggtg atttgaaaaa tataaaatta tgagattggt tttcctgtgg cataaattgc 3420 atcactgtat cattttcttt tttaaccggt aagagtttca gtttgttgga aagtaactgt 3480 gagaacccag tttcccgtcc atctccctta gggactaccc atagacatga aaggtcccca 3540 cagagcaaga gataagtctt tcatggctgc tgttgcttaa accacttaaa cgaagagttc 3600 ccttgaaact ttgggaaaac atgttaatga caatattcca gatctttcag aaatataaca 3660 catttttttg catgcatgca aatgagctct gaaatcttcc catgcattct ggtcaagggc 3720 tgtcattgca cataagcttc cattttaatt ttaaagtgca aaagggccag cgtggctcta 3780 aaaggtaatg tgtggattgc ctctgaaaag tgtgtatata ttttgtgtga aattgcatac 3840 tttgtatttt gattattttt tttttcttct tgggatagtg ggatttccag aaccacactt 3900 gaaacctttt tttatcgttt ttgtattttc atgaaaatac catttagtaa gaataccaca 3960 tcaaataaga aataatgcta caattttaag aggggaggga agggaaagtt tttttttatt 4020 atttttttaa aattttgtat gttaaagaga atgagtcctt gatttcaaag ttttgttgta 4080 cttaaatggt aataagcact gtaaacttct gcaacaagca tgcagctttg caaacccatt 4140 aaggggaaga atgaaagctg ttccttggtc ctagtaagaa gacaaactgc ttcccttact 4200 ttgctgaggg tttgaataaa cctaggactt ccgagctatg tcagtactat tcaggtaaca 4260 ctagggcctt ggaaattcct gtactgtgtc tcatggattt ggcactagcc aaagcgaggc 4320 acccttactg gcttacctcc tcatggcagc ctactctcct tgagtgtatg agtagccagg 4380 gtaaggggta aaaggatagt aagcatagaa accactagaa agtgggctta atggagttct 4440 tgtggcctca gctcaatgca gttagctgaa gaattgaaaa gtttttgttt ggagacgttt 4500 ataaacagaa atggaaagca gagttttcat taaatccttt tacctttttt ttttcttggt 4560 aatcccctaa aataacagta tgtgggatat tgaatgttaa agggatattt tttttctatt 4620 atttttataa ttgtacaaaa ttaagcaaat gttaaaagtt ttatatgctt tattaatgtt 4680 ttcaaaaggt attatacatg tgatacattt tttaagcttc agttgcttgt cttctggtac 4740 tttctgttat gggcttttgg ggagccagaa gccaatctac aatctctttt tgtttgccag 4800 gacatgcaat aaaatttaaa aaataaataa aaactaatta agaaataaa 4849 336 1386 DNA Homo sapiens 336 atgttgtacc tggaaaacaa tgcccagact caatttagtg agccacagta cacgaacctg 60 gggctcctga acagcatgga ccagcagatt cagaacggct cctcgtccac cagtccctat 120 aacacagacc acgcgcagaa cagcgtcacg gcgccctcgc cctacgcaca gcccagctcc 180 accttcgatg ctctctctcc atcacccgcc atcccctcca acaccgacta cccaggcccg 240 cacagtttcg acgtgtcctt ccagcagtcg agcaccgcca agtcggccac ctggacgtat 300 tccactgaac tgaagaaact ctactgccaa attgcaaaga catgccccat ccagatcaag 360 gtgatgaccc cacctcctca gggagctgtt atccgcgcca tgcctgtcta caaaaaagct 420 gagcacgtca cggaggtggt gaagcggtgc cccaaccatg agctgagccg tgaattcaac 480 gagggacaga ttgcccctcc tagtcatttg attcgagtag aggggaacag ccatgcccag 540 tatgtagaag atcccatcac aggaagacag agtgtgctgg taccttatga gccaccccag 600 gttggcactg aattcacgac agtcttgtac aatttcatgt gtaacagcag ttgtgttgga 660 gggatgaacc gccgtccaat tttaatcatt gttactctgg aaaccagaga tgggcaagtc 720 ctgggccgac gctgctttga ggcccggatc tgtgcttgcc caggaagaga caggaaggcg 780 gatgaagata gcatcagaaa gcagcaagtt tcggacagta caaagaacgg tgatggtacg 840 aagcgcccgt ttcgtcagaa cacacatggt atccagatga catccatcaa gaaacgaaga 900 tccccagatg atgaactgtt atacttacca gtgaggggcc gtgagactta tgaaatgctg 960 ttgaagatca aagagtccct ggaactcatg cagtaccttc ctcagcacac aattgaaacg 1020 tacaggcaac agcaacagca gcagcaccag cacttacttc agaaacagac ctcaatacag 1080 tctccatctt catatggtaa cagctcccca cctctgaaca aaatgaacag catgaacaag 1140 ctgccttctg tgagccagct tatcaaccct cagcagcgca acgccctcac tcctacaacc 1200 attcctgatg gcatgggagc caacattccc atgatgggca cccacatgcc aatggctgga 1260 gacatgaatg gactcagccc cacccaggca ctccctcccc cactctccat gccatccacc 1320 tcccactgca cacccccacc tccgtatccc acagattgca gcattgtcag gatctggcaa 1380 gtctga 1386 337 1551 DNA Homo sapiens 337 atgtcccaga gcacacagac aaatgaattc ctcagtccag aggttttcca gcatatctgg 60 gattttctgg aacagcctat atgttcagtt cagcccattg acttgaactt tgtggatgaa 120 ccatcagaag atggtgcgac aaacaagatt gagattagca tggactgtat ccgcatgcag 180 gactcggacc tgagtgaccc catgtggcca cagtacacga acctggggct cctgaacagc 240 atggaccagc agattcagaa cggctcctcg tccaccagtc cctataacac agaccacgcg 300 cagaacagcg tcacggcgcc ctcgccctac gcacagccca gctccacctt cgatgctctc 360 tctccatcac ccgccatccc ctccaacacc gactacccag gcccgcacag tttcgacgtg 420 tccttccagc agtcgagcac cgccaagtcg gccacctgga cgtattccac tgaactgaag 480 aaactctact gccaaattgc aaagacatgc cccatccaga tcaaggtgat gaccccacct 540 cctcagggag ctgttatccg cgccatgcct gtctacaaaa aagctgagca cgtcacggag 600 gtggtgaagc ggtgccccaa ccatgagctg agccgtgaat tcaacgaggg acagattgcc 660 cctcctagtc atttgattcg agtagagggg aacagccatg cccagtatgt agaagatccc 720 atcacaggaa gacagagtgt gctggtacct tatgagccac cccaggttgg cactgaattc 780 acgacagtct tgtacaattt catgtgtaac agcagttgtg ttggagggat gaaccgccgt 840 ccaattttaa tcattgttac tctggaaacc agagatgggc aagtcctggg ccgacgctgc 900 tttgaggccc ggatctgtgc ttgcccagga agagacagga aggcggatga agatagcatc 960 agaaagcagc aagtttcgga cagtacaaag aacggtgatg gtacgaagcg cccgtttcgt 1020 cagaacacac atggtatcca gatgacatcc atcaagaaac gaagatcccc agatgatgaa 1080 ctgttatact taccagtgag gggccgtgag acttatgaaa tgctgttgaa gatcaaagag 1140 tccctggaac tcatgcagta ccttcctcag cacacaattg aaacgtacag gcaacagcaa 1200 cagcagcagc accagcactt acttcagaaa cagacctcaa tacagtctcc atcttcatat 1260 ggtaacagct ccccacctct gaacaaaatg aacagcatga acaagctgcc ttctgtgagc 1320 cagcttatca accctcagca gcgcaacgcc ctcactccta caaccattcc tgatggcatg 1380 ggagccaaca ttcccatgat gggcacccac atgccaatgg ctggagacat gaatggactc 1440 agccccaccc aggcactccc tcccccactc tccatgccat ccacctccca ctgcacaccc 1500 ccacctccgt atcccacaga ttgcagcatt gtcaggatct ggcaagtctg a 1551 338 586 PRT Homo sapiens 338 Met Leu Tyr Leu Glu Asn Asn Ala Gln Thr Gln Phe Ser Glu Pro Gln 5 10 15 Tyr Thr Asn Leu Gly Leu Leu Asn Ser Met Asp Gln Gln Ile Arg Asn 20 25 30 Gly Ser Ser Ser Thr Ser Pro Tyr Asn Thr Asp His Ala Gln Asn Ser 35 40 45 Val Thr Ala Pro Ser Pro Tyr Ala Gln Pro Ser Pro Thr Phe Asp Ala 50 55 60 Leu Ser Pro Ser Pro Ala Ile Pro Ser Asn Thr Asp Tyr Pro Gly Pro 65 70 75 80 His Ser Ser Asp Val Ser Phe Gln Gln Ser Ser Thr Ala Lys Ser Ala 85 90 95 Thr Trp Thr Tyr Ser Thr Glu Leu Lys Lys Leu Tyr Cys Gln Ile Ala 100 105 110 Lys Thr Cys Pro Ile Gln Ile Lys Val Met Thr Pro Pro Pro Gln Gly 115 120 125 Ala Val Ile Arg Ala Met Pro Val Tyr Lys Lys Ala Glu His Val Thr 130 135 140 Glu Val Val Lys Arg Cys Pro Asn His Glu Leu Ser Arg Glu Phe Asn 145 150 155 160 Glu Gly Gln Ile Ala Pro Pro Ser His Leu Ile Arg Val Glu Gly Asn 165 170 175 Ser His Ala Gln Tyr Val Glu Asp Pro Ile Thr Gly Arg Gln Ser Val 180 185 190 Leu Val Pro Tyr Glu Pro Pro Gln Val Gly Thr Glu Phe Thr Thr Val 195 200 205 Leu Tyr Asn Phe Met Cys Asn Ser Ser Cys Val Gly Gly Met Asn Arg 210 215 220 Arg Pro Ile Leu Ile Ile Val Thr Leu Glu Thr Arg Asp Gly Gln Val 225 230 235 240 Leu Gly Arg Arg Cys Phe Glu Ala Arg Ile Cys Ala Cys Pro Gly Arg 245 250 255 Asp Arg Lys Ala Asp Glu Asp Ser Ile Arg Lys Gln Gln Val Ser Asp 260 265 270 Ser Thr Lys Asn Gly Asp Gly Thr Lys Arg Pro Phe Arg Gln Asn Thr 275 280 285 His Gly Ile Gln Met Thr Ser Ile Lys Lys Arg Arg Ser Pro Asp Asp 290 295 300 Glu Leu Leu Tyr Leu Pro Val Arg Gly Arg Glu Thr Tyr Glu Met Leu 305 310 315 320 Leu Lys Ile Lys Glu Ser Leu Glu Leu Met Gln Tyr Leu Pro Gln His 325 330 335 Thr Ile Glu Thr Tyr Arg Gln Gln Gln Gln Gln Gln His Gln His Leu 340 345 350 Leu Gln Lys Gln Thr Ser Ile Gln Ser Pro Ser Ser Tyr Gly Asn Ser 355 360 365 Ser Pro Pro Leu Asn Lys Met Asn Ser Met Asn Lys Leu Pro Ser Val 370 375 380 Ser Gln Leu Ile Asn Pro Gln Gln Arg Asn Ala Leu Thr Pro Thr Thr 385 390 395 400 Ile Pro Asp Gly Met Gly Ala Asn Ile Pro Met Met Gly Thr His Met 405 410 415 Pro Met Ala Gly Asp Met Asn Gly Leu Ser Pro Thr Gln Ala Leu Pro 420 425 430 Pro Pro Leu Ser Met Pro Ser Thr Ser His Cys Thr Pro Pro Pro Pro 435 440 445 Tyr Pro Thr Asp Cys Ser Ile Val Ser Phe Leu Ala Arg Leu Gly Cys 450 455 460 Ser Ser Cys Leu Asp Tyr Phe Thr Thr Gln Gly Leu Thr Thr Ile Tyr 465 470 475 480 Gln Ile Glu His Tyr Ser Met Asp Asp Leu Ala Ser Leu Lys Ile Pro 485 490 495 Glu Gln Phe Arg His Ala Ile Trp Lys Gly Ile Leu Asp His Arg Gln 500 505 510 Leu His Glu Phe Ser Ser Pro Ser His Leu Leu Arg Thr Pro Ser Ser 515 520 525 Ala Ser Thr Val Ser Val Gly Ser Ser Glu Thr Arg Gly Glu Arg Val 530 535 540 Ile Asp Ala Val Arg Phe Thr Leu Arg Gln Thr Ile Ser Phe Pro Pro 545 550 555 560 Arg Asp Glu Trp Asn Asp Phe Asn Phe Asp Met Asp Ala Arg Arg Asn 565 570 575 Lys Gln Gln Arg Ile Lys Glu Glu Gly Glu 580 585 339 641 PRT Homo sapiens 339 Met Ser Gln Ser Thr Gln Thr Asn Glu Phe Leu Ser Pro Glu Val Phe 5 10 15 Gln His Ile Trp Asp Phe Leu Glu Gln Pro Ile Cys Ser Val Gln Pro 20 25 30 Ile Asp Leu Asn Phe Val Asp Glu Pro Ser Glu Asp Gly Ala Thr Asn 35 40 45 Lys Ile Glu Ile Ser Met Asp Cys Ile Arg Met Gln Asp Ser Asp Leu 50 55 60 Ser Asp Pro Met Trp Pro Gln Tyr Thr Asn Leu Gly Leu Leu Asn Ser 65 70 75 80 Met Asp Gln Gln Ile Gln Asn Gly Ser Ser Ser Thr Ser Pro Tyr Asn 85 90 95 Thr Asp His Ala Gln Asn Ser Val Thr Ala Pro Ser Pro Tyr Ala Gln 100 105 110 Pro Ser Ser Thr Phe Asp Ala Leu Ser Pro Ser Pro Ala Ile Pro Ser 115 120 125 Asn Thr Asp Tyr Pro Gly Pro His Ser Phe Asp Val Ser Phe Gln Gln 130 135 140 Ser Ser Thr Ala Lys Ser Ala Thr Trp Thr Tyr Ser Thr Glu Leu Lys 145 150 155 160 Lys Leu Tyr Cys Gln Ile Ala Lys Thr Cys Pro Ile Gln Ile Lys Val 165 170 175 Met Thr Pro Pro Pro Gln Gly Ala Val Ile Arg Ala Met Pro Val Tyr 180 185 190 Lys Lys Ala Glu His Val Thr Glu Val Val Lys Arg Cys Pro Asn His 195 200 205 Glu Leu Ser Arg Glu Phe Asn Glu Gly Gln Ile Ala Pro Pro Ser His 210 215 220 Leu Ile Arg Val Glu Gly Asn Ser His Ala Gln Tyr Val Glu Asp Pro 225 230 235 240 Ile Thr Gly Arg Gln Ser Val Leu Val Pro Tyr Glu Pro Pro Gln Val 245 250 255 Gly Thr Glu Phe Thr Thr Val Leu Tyr Asn Phe Met Cys Asn Ser Ser 260 265 270 Cys Val Gly Gly Met Asn Arg Arg Pro Ile Leu Ile Ile Val Thr Leu 275 280 285 Glu Thr Arg Asp Gly Gln Val Leu Gly Arg Arg Cys Phe Glu Ala Arg 290 295 300 Ile Cys Ala Cys Pro Gly Arg Asp Arg Lys Ala Asp Glu Asp Ser Ile 305 310 315 320 Arg Lys Gln Gln Val Ser Asp Ser Thr Lys Asn Gly Asp Gly Thr Lys 325 330 335 Arg Pro Phe Arg Gln Asn Thr His Gly Ile Gln Met Thr Ser Ile Lys 340 345 350 Lys Arg Arg Ser Pro Asp Asp Glu Leu Leu Tyr Leu Pro Val Arg Gly 355 360 365 Arg Glu Thr Tyr Glu Met Leu Leu Lys Ile Lys Glu Ser Leu Glu Leu 370 375 380 Met Gln Tyr Leu Pro Gln His Thr Ile Glu Thr Tyr Arg Gln Gln Gln 385 390 395 400 Gln Gln Gln His Gln His Leu Leu Gln Lys Gln Thr Ser Ile Gln Ser 405 410 415 Pro Ser Ser Tyr Gly Asn Ser Ser Pro Pro Leu Asn Lys Met Asn Ser 420 425 430 Met Asn Lys Leu Pro Ser Val Ser Gln Leu Ile Asn Pro Gln Gln Arg 435 440 445 Asn Ala Leu Thr Pro Thr Thr Ile Pro Asp Gly Met Gly Ala Asn Ile 450 455 460 Pro Met Met Gly Thr His Met Pro Met Ala Gly Asp Met Asn Gly Leu 465 470 475 480 Ser Pro Thr Gln Ala Leu Pro Pro Pro Leu Ser Met Pro Ser Thr Ser 485 490 495 His Cys Thr Pro Pro Pro Pro Tyr Pro Thr Asp Cys Ser Ile Val Gly 500 505 510 Phe Leu Ala Arg Leu Gly Cys Ser Ser Cys Leu Asp Tyr Phe Thr Thr 515 520 525 Gln Gly Leu Thr Thr Ile Tyr Gln Ile Glu His Tyr Ser Met Asp Asp 530 535 540 Leu Ala Ser Leu Lys Ile Pro Glu Gln Phe Arg His Ala Ile Trp Lys 545 550 555 560 Gly Ile Leu Asp His Arg Gln Leu His Glu Phe Ser Ser Pro Ser His 565 570 575 Leu Leu Arg Thr Pro Ser Ser Ala Ser Thr Val Ser Val Gly Ser Ser 580 585 590 Glu Thr Arg Gly Glu Arg Val Ile Asp Ala Val Arg Phe Thr Leu Arg 595 600 605 Gln Thr Ile Ser Phe Pro Pro Arg Asp Glu Trp Asn Asp Phe Asn Phe 610 615 620 Asp Met Asp Ala Arg Arg Asn Lys Gln Gln Arg Ile Lys Glu Glu Gly 625 630 635 640 Glu 340 448 PRT Homo sapiens 340 Met Ser Gln Ser Thr Gln Thr Asn Glu Phe Leu Ser Pro Glu Val Phe 5 10 15 Gln His Ile Trp Asp Phe Leu Glu Gln Pro Ile Cys Ser Val Gln Pro 20 25 30 Ile Asp Leu Asn Phe Val Asp Glu Pro Ser Glu Asp Gly Ala Thr Asn 35 40 45 Lys Ile Glu Ile Ser Met Asp Cys Ile Arg Met Gln Asp Ser Asp Leu 50 55 60 Ser Asp Pro Met Trp Pro Gln Tyr Thr Asn Leu Gly Leu Leu Asn Ser 65 70 75 80 Met Asp Gln Gln Ile Gln Asn Gly Ser Ser Ser Thr Ser Pro Tyr Asn 85 90 95 Thr Asp His Ala Gln Asn Ser Val Thr Ala Pro Ser Pro Tyr Ala Gln 100 105 110 Pro Ser Ser Thr Phe Asp Ala Leu Ser Pro Ser Pro Ala Ile Pro Ser 115 120 125 Asn Thr Asp Tyr Pro Gly Pro His Ser Phe Asp Val Ser Phe Gln Gln 130 135 140 Ser Ser Thr Ala Lys Ser Ala Thr Trp Thr Tyr Ser Thr Glu Leu Lys 145 150 155 160 Lys Leu Tyr Cys Gln Ile Ala Lys Thr Cys Pro Ile Gln Ile Lys Val 165 170 175 Met Thr Pro Pro Pro Gln Gly Ala Val Ile Arg Ala Met Pro Val Tyr 180 185 190 Lys Lys Ala Glu His Val Thr Glu Val Val Lys Arg Cys Pro Asn His 195 200 205 Glu Leu Ser Arg Glu Phe Asn Glu Gly Gln Ile Ala Pro Pro Ser His 210 215 220 Leu Ile Arg Val Glu Gly Asn Ser His Ala Gln Tyr Val Glu Asp Pro 225 230 235 240 Ile Thr Gly Arg Gln Ser Val Leu Val Pro Tyr Glu Pro Pro Gln Val 245 250 255 Gly Thr Glu Phe Thr Thr Val Leu Tyr Asn Phe Met Cys Asn Ser Ser 260 265 270 Cys Val Gly Gly Met Asn Arg Arg Pro Ile Leu Ile Ile Val Thr Leu 275 280 285 Glu Thr Arg Asp Gly Gln Val Leu Gly Arg Arg Cys Phe Glu Ala Arg 290 295 300 Ile Cys Ala Cys Pro Gly Arg Asp Arg Lys Ala Asp Glu Asp Ser Ile 305 310 315 320 Arg Lys Gln Gln Val Ser Asp Ser Thr Lys Asn Gly Asp Gly Thr Lys 325 330 335 Arg Pro Phe Arg Gln Asn Thr His Gly Ile Gln Met Thr Ser Ile Lys 340 345 350 Lys Arg Arg Ser Pro Asp Asp Glu Leu Leu Tyr Leu Pro Val Arg Gly 355 360 365 Arg Glu Thr Tyr Glu Met Leu Leu Lys Ile Lys Glu Ser Leu Glu Leu 370 375 380 Met Gln Tyr Leu Pro Gln His Thr Ile Glu Thr Tyr Arg Gln Gln Gln 385 390 395 400 Gln Gln Gln His Gln His Leu Leu Gln Lys His Leu Leu Ser Ala Cys 405 410 415 Phe Arg Asn Glu Leu Val Glu Pro Arg Arg Glu Thr Pro Lys Gln Ser 420 425 430 Asp Val Phe Phe Arg His Ser Lys Pro Pro Asn Arg Ser Val Tyr Pro 435 440 445 341 356 PRT Homo sapiens 341 Met Leu Tyr Leu Glu Asn Asn Ala Gln Thr Gln Phe Ser Glu Pro Gln 5 10 15 Tyr Thr Asn Leu Gly Leu Leu Asn Ser Met Asp Gln Gln Ile Gln Asn 20 25 30 Gly Ser Ser Ser Thr Ser Pro Tyr Asn Thr Asp His Ala Gln Asn Ser 35 40 45 Val Thr Ala Pro Ser Pro Tyr Ala Gln Pro Ser Ser Thr Phe Asp Ala 50 55 60 Leu Ser Pro Ser Pro Ala Ile Pro Ser Asn Thr Asp Tyr Pro Gly Pro 65 70 75 80 His Ser Phe Asp Val Ser Phe Gln Gln Ser Ser Thr Ala Lys Ser Ala 85 90 95 Thr Trp Thr Tyr Ser Thr Glu Leu Lys Lys Leu Tyr Cys Gln Ile Ala 100 105 110 Lys Thr Cys Pro Ile Gln Ile Lys Val Met Thr Pro Pro Pro Gln Gly 115 120 125 Ala Val Ile Arg Ala Met Pro Val Tyr Lys Lys Ala Glu His Val Thr 130 135 140 Glu Val Val Lys Arg Cys Pro Asn His Glu Leu Ser Arg Glu Phe Asn 145 150 155 160 Glu Gly Gln Ile Ala Pro Pro Ser His Leu Ile Arg Val Glu Gly Asn 165 170 175 Ser His Ala Gln Tyr Val Glu Asp Pro Ile Thr Gly Arg Gln Ser Val 180 185 190 Leu Val Pro Tyr Glu Pro Pro Gln Val Gly Thr Glu Phe Thr Thr Val 195 200 205 Leu Tyr Asn Phe Met Cys Asn Ser Ser Cys Val Gly Gly Met Asn Arg 210 215 220 Arg Pro Ile Leu Ile Ile Val Thr Leu Glu Thr Arg Asp Gly Gln Val 225 230 235 240 Leu Gly Arg Arg Cys Phe Glu Ala Arg Ile Cys Ala Cys Pro Gly Arg 245 250 255 Asp Arg Lys Ala Asp Glu Asp Ser Ile Arg Lys Gln Gln Val Ser Asp 260 265 270 Ser Thr Lys Asn Gly Asp Gly Thr Lys Arg Pro Ser Arg Gln Asn Thr 275 280 285 His Gly Ile Gln Met Thr Ser Ile Lys Lys Arg Arg Ser Pro Asp Asp 290 295 300 Glu Leu Leu Tyr Leu Pro Val Arg Gly Arg Glu Thr Tyr Glu Met Leu 305 310 315 320 Leu Lys Ile Lys Glu Ser Leu Glu Leu Met Gln Tyr Leu Pro Gln His 325 330 335 Thr Ile Glu Thr Tyr Arg Gln Gln Gln Gln Gln Gln His Gln His Leu 340 345 350 Leu Gln Lys Gln 355 342 680 PRT Homo sapiens 342 Met Asn Phe Glu Thr Ser Arg Cys Ala Thr Leu Gln Tyr Cys Pro Asp 5 10 15 Pro Tyr Ile Gln Arg Phe Val Glu Thr Pro Ala His Phe Ser Trp Lys 20 25 30 Glu Ser Tyr Tyr Arg Ser Thr Met Ser Gln Ser Thr Gln Thr Asn Glu 35 40 45 Phe Leu Ser Pro Glu Val Phe Gln His Ile Trp Asp Phe Leu Glu Gln 50 55 60 Pro Ile Cys Ser Val Gln Pro Ile Asp Leu Asn Phe Val Asp Glu Pro 65 70 75 80 Ser Glu Asp Gly Ala Thr Asn Lys Ile Glu Ile Ser Met Asp Cys Ile 85 90 95 Arg Met Gln Asp Ser Asp Leu Ser Asp Pro Met Trp Pro Gln Tyr Thr 100 105 110 Asn Leu Gly Leu Leu Asn Ser Met Asp Gln Gln Ile Gln Asn Gly Ser 115 120 125 Ser Ser Thr Ser Pro Tyr Asn Thr Asp His Ala Gln Asn Ser Val Thr 130 135 140 Ala Pro Ser Pro Tyr Ala Gln Pro Ser Ser Thr Phe Asp Ala Leu Ser 145 150 155 160 Pro Ser Pro Ala Ile Pro Ser Asn Thr Asp Tyr Pro Gly Pro His Ser 165 170 175 Phe Asp Val Ser Phe Gln Gln Ser Ser Thr Ala Lys Ser Ala Thr Trp 180 185 190 Thr Tyr Ser Thr Glu Leu Lys Lys Leu Tyr Cys Gln Ile Ala Lys Thr 195 200 205 Cys Pro Ile Gln Ile Lys Val Met Thr Pro Pro Pro Gln Gly Ala Val 210 215 220 Ile Arg Ala Met Pro Val Tyr Lys Lys Ala Glu His Val Thr Glu Val 225 230 235 240 Val Lys Arg Cys Pro Asn His Glu Leu Ser Arg Glu Phe Asn Glu Gly 245 250 255 Gln Ile Ala Pro Pro Ser His Leu Ile Arg Val Glu Gly Asn Ser His 260 265 270 Ala Gln Tyr Val Glu Asp Pro Ile Thr Gly Arg Gln Ser Val Leu Val 275 280 285 Pro Tyr Glu Pro Pro Gln Val Gly Thr Glu Phe Thr Thr Val Leu Tyr 290 295 300 Asn Phe Met Cys Asn Ser Ser Cys Val Gly Gly Met Asn Arg Arg Pro 305 310 315 320 Ile Leu Ile Ile Val Thr Leu Glu Thr Arg Asp Gly Gln Val Leu Gly 325 330 335 Arg Arg Cys Phe Glu Ala Arg Ile Cys Ala Cys Pro Gly Arg Asp Arg 340 345 350 Lys Ala Asp Glu Asp Ser Ile Arg Lys Gln Gln Val Ser Asp Ser Thr 355 360 365 Lys Asn Gly Asp Gly Thr Lys Arg Pro Phe Arg Gln Asn Thr His Gly 370 375 380 Ile Gln Met Thr Ser Ile Lys Lys Arg Arg Ser Pro Asp Asp Glu Leu 385 390 395 400 Leu Tyr Leu Pro Val Arg Gly Arg Glu Thr Tyr Glu Met Leu Leu Lys 405 410 415 Ile Lys Glu Ser Leu Glu Leu Met Gln Tyr Leu Pro Gln His Thr Ile 420 425 430 Glu Thr Tyr Arg Gln Gln Gln Gln Gln Gln His Gln His Leu Leu Gln 435 440 445 Lys Gln Thr Ser Ile Gln Ser Pro Ser Ser Tyr Gly Asn Ser Ser Pro 450 455 460 Pro Leu Asn Lys Met Asn Ser Met Asn Lys Leu Pro Ser Val Ser Gln 465 470 475 480 Leu Ile Asn Pro Gln Gln Arg Asn Ala Leu Thr Pro Thr Thr Ile Pro 485 490 495 Asp Gly Met Gly Ala Asn Ile Pro Met Met Gly Thr His Met Pro Met 500 505 510 Ala Gly Asp Met Asn Gly Leu Ser Pro Thr Gln Ala Leu Pro Pro Pro 515 520 525 Leu Ser Met Pro Ser Thr Ser Gln Cys Thr Pro Pro Pro Pro Tyr Pro 530 535 540 Thr Asp Cys Ser Ile Val Ser Phe Leu Ala Arg Leu Gly Cys Ser Ser 545 550 555 560 Cys Leu Asp Tyr Phe Thr Thr Gln Gly Leu Thr Thr Ile Tyr Gln Ile 565 570 575 Glu His Tyr Ser Met Asp Asp Leu Ala Ser Leu Lys Ile Pro Glu Gln 580 585 590 Phe Arg His Ala Ile Trp Lys Gly Ile Leu Asp His Arg Gln Leu His 595 600 605 Glu Phe Ser Ser Pro Ser His Leu Leu Arg Thr Pro Ser Ser Ala Ser 610 615 620 Thr Val Ser Val Gly Ser Ser Glu Thr Arg Gly Glu Arg Val Ile Asp 625 630 635 640 Ala Val Arg Phe Thr Leu Arg Gln Thr Ile Ser Phe Pro Pro Arg Asp 645 650 655 Glu Trp Asn Asp Phe Asn Phe Asp Met Asp Ala Arg Arg Asn Lys Gln 660 665 670 Gln Arg Ile Lys Glu Glu Gly Glu 675 680 343 461 PRT Homo sapiens 343 Met Leu Tyr Leu Glu Asn Asn Ala Gln Thr Gln Phe Ser Glu Pro Gln 5 10 15 Tyr Thr Asn Leu Gly Leu Leu Asn Ser Met Asp Gln Gln Ile Gln Asn 20 25 30 Gly Ser Ser Ser Thr Ser Pro Tyr Asn Thr Asp His Ala Gln Asn Ser 35 40 45 Val Thr Ala Pro Ser Pro Tyr Ala Gln Pro Ser Ser Thr Phe Asp Ala 50 55 60 Leu Ser Pro Ser Pro Ala Ile Pro Ser Asn Thr Asp Tyr Pro Gly Pro 65 70 75 80 His Ser Phe Asp Val Ser Phe Gln Gln Ser Ser Thr Ala Lys Ser Ala 85 90 95 Thr Trp Thr Tyr Ser Thr Glu Leu Lys Lys Leu Tyr Cys Gln Ile Ala 100 105 110 Lys Thr Cys Pro Ile Gln Ile Lys Val Met Thr Pro Pro Pro Gln Gly 115 120 125 Ala Val Ile Arg Ala Met Pro Val Tyr Lys Lys Ala Glu His Val Thr 130 135 140 Glu Val Val Lys Arg Cys Pro Asn His Glu Leu Ser Arg Glu Phe Asn 145 150 155 160 Glu Gly Gln Ile Ala Pro Pro Ser His Leu Ile Arg Val Glu Gly Asn 165 170 175 Ser His Ala Gln Tyr Val Glu Asp Pro Ile Thr Gly Arg Gln Ser Val 180 185 190 Leu Val Pro Tyr Glu Pro Pro Gln Val Gly Thr Glu Phe Thr Thr Val 195 200 205 Leu Tyr Asn Phe Met Cys Asn Ser Ser Cys Val Gly Gly Met Asn Arg 210 215 220 Arg Pro Ile Leu Ile Ile Val Thr Leu Glu Thr Arg Asp Gly Gln Val 225 230 235 240 Leu Gly Arg Arg Cys Phe Glu Ala Arg Ile Cys Ala Cys Pro Gly Arg 245 250 255 Asp Arg Lys Ala Asp Glu Asp Ser Ile Arg Lys Gln Gln Val Ser Asp 260 265 270 Ser Thr Lys Asn Gly Asp Gly Thr Lys Arg Pro Phe Arg Gln Asn Thr 275 280 285 His Gly Ile Gln Met Thr Ser Ile Lys Lys Arg Arg Ser Pro Asp Asp 290 295 300 Glu Leu Leu Tyr Leu Pro Val Arg Gly Arg Glu Thr Tyr Glu Met Leu 305 310 315 320 Leu Lys Ile Lys Glu Ser Leu Glu Leu Met Gln Tyr Leu Pro Gln His 325 330 335 Thr Ile Glu Thr Tyr Arg Gln Gln Gln Gln Gln Gln His Gln His Leu 340 345 350 Leu Gln Lys Gln Thr Ser Ile Gln Ser Pro Ser Ser Tyr Gly Asn Ser 355 360 365 Ser Pro Pro Leu Asn Lys Met Asn Ser Met Asn Lys Leu Pro Ser Val 370 375 380 Ser Gln Leu Ile Asn Pro Gln Gln Arg Asn Ala Leu Thr Pro Thr Thr 385 390 395 400 Ile Pro Asp Gly Met Gly Ala Asn Ile Pro Met Met Gly Thr His Met 405 410 415 Pro Met Ala Gly Asp Met Asn Gly Leu Ser Pro Thr Gln Ala Leu Pro 420 425 430 Pro Pro Leu Ser Met Pro Ser Thr Ser His Cys Thr Pro Pro Pro Pro 435 440 445 Tyr Pro Thr Asp Cys Ser Ile Val Arg Ile Trp Gln Val 450 455 460 344 516 PRT Homo sapiens 344 Met Ser Gln Ser Thr Gln Thr Asn Glu Phe Leu Ser Pro Glu Val Phe 5 10 15 Gln His Ile Trp Asp Phe Leu Glu Gln Pro Ile Cys Ser Val Gln Pro 20 25 30 Ile Asp Leu Asn Phe Val Asp Glu Pro Ser Glu Asp Gly Ala Thr Asn 35 40 45 Lys Ile Glu Ile Ser Met Asp Cys Ile Arg Met Gln Asp Ser Asp Leu 50 55 60 Ser Asp Pro Met Trp Pro Gln Tyr Thr Asn Leu Gly Leu Leu Asn Ser 65 70 75 80 Met Asp Gln Gln Ile Gln Asn Gly Ser Ser Ser Thr Ser Pro Tyr Asn 85 90 95 Thr Asp His Ala Gln Asn Ser Val Thr Ala Pro Ser Pro Tyr Ala Gln 100 105 110 Pro Ser Ser Thr Phe Asp Ala Leu Ser Pro Ser Pro Ala Ile Pro Ser 115 120 125 Asn Thr Asp Tyr Pro Gly Pro His Ser Phe Asp Val Ser Phe Gln Gln 130 135 140 Ser Ser Thr Ala Lys Ser Ala Thr Trp Thr Tyr Ser Thr Glu Leu Lys 145 150 155 160 Lys Leu Tyr Cys Gln Ile Ala Lys Thr Cys Pro Ile Gln Ile Lys Val 165 170 175 Met Thr Pro Pro Pro Gln Gly Ala Val Ile Arg Ala Met Pro Val Tyr 180 185 190 Lys Lys Ala Glu His Val Thr Glu Val Val Lys Arg Cys Pro Asn His 195 200 205 Glu Leu Ser Arg Glu Phe Asn Glu Gly Gln Ile Ala Pro Pro Ser His 210 215 220 Leu Ile Arg Val Glu Gly Asn Ser His Ala Gln Tyr Val Glu Asp Pro 225 230 235 240 Ile Thr Gly Arg Gln Ser Val Leu Val Pro Tyr Glu Pro Pro Gln Val 245 250 255 Gly Thr Glu Phe Thr Thr Val Leu Tyr Asn Phe Met Cys Asn Ser Ser 260 265 270 Cys Val Gly Gly Met Asn Arg Arg Pro Ile Leu Ile Ile Val Thr Leu 275 280 285 Glu Thr Arg Asp Gly Gln Val Leu Gly Arg Arg Cys Phe Glu Ala Arg 290 295 300 Ile Cys Ala Cys Pro Gly Arg Asp Arg Lys Ala Asp Glu Asp Ser Ile 305 310 315 320 Arg Lys Gln Gln Val Ser Asp Ser Thr Lys Asn Gly Asp Gly Thr Lys 325 330 335 Arg Pro Phe Arg Gln Asn Thr His Gly Ile Gln Met Thr Ser Ile Lys 340 345 350 Lys Arg Arg Ser Pro Asp Asp Glu Leu Leu Tyr Leu Pro Val Arg Gly 355 360 365 Arg Glu Thr Tyr Glu Met Leu Leu Lys Ile Lys Glu Ser Leu Glu Leu 370 375 380 Met Gln Tyr Leu Pro Gln His Thr Ile Glu Thr Tyr Arg Gln Gln Gln 385 390 395 400 Gln Gln Gln His Gln His Leu Leu Gln Lys Gln Thr Ser Ile Gln Ser 405 410 415 Pro Ser Ser Tyr Gly Asn Ser Ser Pro Pro Leu Asn Lys Met Asn Ser 420 425 430 Met Asn Lys Leu Pro Ser Val Ser Gln Leu Ile Asn Pro Gln Gln Arg 435 440 445 Asn Ala Leu Thr Pro Thr Thr Ile Pro Asp Gly Met Gly Ala Asn Ile 450 455 460 Pro Met Met Gly Thr His Met Pro Met Ala Gly Asp Met Asn Gly Leu 465 470 475 480 Ser Pro Thr Gln Ala Leu Pro Pro Pro Leu Ser Met Pro Ser Thr Ser 485 490 495 His Cys Thr Pro Pro Pro Pro Tyr Pro Thr Asp Cys Ser Ile Val Arg 500 505 510 Ile Trp Gln Val 515 345 1800 DNA Homo sapiens 345 gcgcctcatt gccactgcag tgactaaagc tgggaagacg ctggtcagtt cacctgcccc 60 actggttgtt ttttaaacaa attctgatac aggcgacatc ctcactgacc gagcaaagat 120 tgacattcgt atcatcactg tgcaccattg gcttctaggc actccagtgg ggtaggagaa 180 ggaggtctga aaccctcgca gagggatctt gccctcattc tttgggtctg aaacactggc 240 agtcgttgga aacaggactc agggataaac cagcgcaatg gattggggga cgctgcacac 300 tttcatcggg ggtgtcaaca aacactccac cagcatcggg aaggtgtgga tcacagtcat 360 ctttattttc cgagtcatga tcctagtggt ggctgcccag gaagtgtggg gtgacgagca 420 agaggacttc gtctgcaaca cactgcaacc gggatgcaaa aatgtgtgct atgaccactt 480 tttcccggtg tcccacatcc ggctgtgggc cctccagctg atcttcgtct ccaccccagc 540 gctgctggtg gccatgcatg tggcctacta caggcacgaa accactcgca agttcaggcg 600 aggagagaag aggaatgatt tcaaagacat agaggacatt aaaaagcaca aggttcggat 660 agaggggtcg ctgtggtgga cgtacaccag cagcatcttt ttccgaatca tctttgaagc 720 agcctttatg tatgtgtttt acttccttta caatgggtac cacctgccct gggtgttgaa 780 atgtgggatt gacccctgcc ccaaccttgt tgactgcttt atttctaggc caacagagaa 840 gaccgtgttt accattttta tgatttctgc gtctgtgatt tgcatgctgc ttaacgtggc 900 agagttgtgc tacctgctgc tgaaagtgtg ttttaggaga tcaaagagag cacagacgca 960 aaaaaatcac cccaatcatg ccctaaagga gagtaagcag aatgaaatga atgagctgat 1020 ttcagatagt ggtcaaaatg caatcacagg tttcccaagc taaacatttc aaggtaaaat 1080 gtagctgcgt cataaggaga cttctgtctt ctccagaagg caataccaac ctgaaagttc 1140 cttctgtagc ctgaagagtt tgtaaatgac tttcataata aatagacact tgagttaact 1200 ttttgtagga tacttgctcc attcatacac aacgtaatca aatatgtggt ccatctctga 1260 aaacaagaga ctgcttgaca aaggagcatt gcagtcactt tgacaggttc cttttaagtg 1320 gactctctga caaagtgggt actttctgaa aatttatata actgttgttg ataaggaaca 1380 tttatccagg aattgatacg tttattagga aaagatattt ttataggctt ggatgttttt 1440 agttccgact ttgaatttat ataaagtatt tttataatga ctggtcttcc ttacctggaa 1500 aaacatgcga tgttagtttt agaattacac cacaagtatc taaatttcca acttacaaag 1560 ggtcctatct tgtaaatatt gttttgcatt gtctgttggc aaatttgtga actgtcatga 1620 tacgcttaag gtgggaaagt gttcattgca caatatattt ttactgcttt ctgaatgtag 1680 acggaacagt gtggaagcag aaggcttttt taactcatcc gtttggccga tcgttgcaga 1740 ccactgggag atgtggatgt ggttgcctcc ttttgctcgt ccccgtggct taacccttct 1800 346 261 PRT Homo sapiens 346 Met Asp Trp Gly Thr Leu His Thr Phe Ile Gly Gly Val Asn Lys His 5 10 15 Ser Thr Ser Ile Gly Lys Val Trp Ile Thr Val Ile Phe Ile Phe Arg 20 25 30 Val Met Ile Leu Val Val Ala Ala Gln Glu Val Trp Gly Asp Glu Gln 35 40 45 Glu Asp Phe Val Cys Asn Thr Leu Gln Pro Gly Cys Lys Asn Val Cys 50 55 60 Tyr Asp His Phe Phe Pro Val Ser His Ile Arg Leu Trp Ala Leu Gln 65 70 75 80 Leu Ile Phe Val Ser Thr Pro Ala Leu Leu Val Ala Met His Val Ala 85 90 95 Tyr Tyr Arg His Glu Thr Thr Arg Lys Phe Arg Arg Gly Glu Lys Arg 100 105 110 Asn Asp Phe Lys Asp Ile Glu Asp Ile Lys Lys His Lys Val Arg Ile 115 120 125 Glu Gly Ser Leu Trp Trp Thr Tyr Thr Ser Ser Ile Phe Phe Arg Ile 130 135 140 Ile Phe Glu Ala Ala Phe Met Tyr Val Phe Tyr Phe Leu Tyr Asn Gly 145 150 155 160 Tyr His Leu Pro Trp Val Leu Lys Cys Gly Ile Asp Pro Cys Pro Asn 165 170 175 Leu Val Asp Cys Phe Ile Ser Arg Pro Thr Glu Lys Thr Val Phe Thr 180 185 190 Ile Phe Met Ile Ser Ala Ser Val Ile Cys Met Leu Leu Asn Val Ala 195 200 205 Glu Leu Cys Tyr Leu Leu Leu Lys Val Cys Phe Arg Arg Ser Lys Arg 210 215 220 Ala Gln Thr Gln Lys Asn His Pro Asn His Ala Leu Lys Glu Ser Lys 225 230 235 240 Gln Asn Glu Met Asn Glu Leu Ile Ser Asp Ser Gly Gln Asn Ala Ile 245 250 255 Thr Gly Phe Pro Ser 260 347 1740 DNA Homo sapiens 347 atgaacaaac tgtatatcgg aaacctcagc gagaacgccg ccccctcgga cctagaaagt 60 atcttcaagg acgccaagat cccggtgtcg ggacccttcc tggtgaagac tggctacgcg 120 ttcgtggact gcccggacga gagctgggcc ctcaaggcca tcgaggcgct ttcaggtaaa 180 atagaactgc acgggaaacc catagaagtt gagcactcgg tcccaaaaag gcaaaggatt 240 cggaaacttc agatacgaaa tatcccgcct catttacagt gggaggtgct ggatagttta 300 ctagtccagt atggagtggt ggagagctgt gagcaagtga acactgactc ggaaactgca 360 gttgtaaatg taacctattc cagtaaggac caagctagac aagcactaga caaactgaat 420 ggatttcagt tagagaattt caccttgaaa gtagcctata tccctgatga aacggccgcc 480 cagcaaaacc ccttgcagca gccccgaggt cgccgggggc ttgggcagag gggctcctca 540 aggcaggggt ctccaggatc cgtatccaag cagaaaccat gtgatttgcc tctgcgcctg 600 ctggttccca cccaatttgt tggagccatc ataggaaaag aaggtgccac cattcggaac 660 atcaccaaac agacccagtc taaaatcgat gtccaccgta aagaaaatgc gggggctgct 720 gagaagtcga ttactatcct ctctactcct gaaggcacct ctgcggcttg taagtctatt 780 ctggagatta tgcataagga agctcaagat ataaaattca cagaagagat ccccttgaag 840 attttagctc ataataactt tgttggacgt cttattggta aagaaggaag aaatcttaaa 900 aaaattgagc aagacacaga cactaaaatc acgatatctc cattgcagga attgacgctg 960 tataatccag aacgcactat tacagttaaa ggcaatgttg agacatgtgc caaagctgag 1020 gaggagatca tgaagaaaat cagggagtct tatgaaaatg atattgcttc tatgaatctt 1080 caagcacatt taattcctgg attaaatctg aacgccttgg gtctgttccc acccacttca 1140 gggatgccac ctcccacctc agggccccct tcagccatga ctcctcccta cccgcagttt 1200 gagcaatcag aaacggagac tgttcatctg tttatcccag ctctatcagt cggtgccatc 1260 atcggcaagc agggccagca catcaagcag ctttctcgct ttgctggagc ttcaattaag 1320 attgctccag cggaagcacc agatgctaaa gtgaggatgg tgattatcac tggaccacca 1380 gaggctcagt tcaaggctca gggaagaatt tatggaaaaa ttaaagaaga aaactttgtt 1440 agtcctaaag aagaggtgaa acttgaagct catatcagag tgccatcctt tgctgctggc 1500 agagttattg gaaaaggagg caaaacggtg aatgaacttc agaatttgtc aagtgcagaa 1560 gttgttgtcc ctcgtgacca gacacctgat gagaatgacc aagtggttgt caaaataact 1620 ggtcacttct atgcttgcca ggttgcccag agaaaaattc aggaaattct gactcaggta 1680 aagcagcacc aacaacagaa ggctctgcaa agtggaccac ctcagtcaag acggaagtaa 1740 348 579 PRT Homo sapiens 348 Met Asn Lys Leu Tyr Ile Gly Asn Leu Ser Glu Asn Ala Ala Pro Ser 5 10 15 Asp Leu Glu Ser Ile Phe Lys Asp Ala Lys Ile Pro Val Ser Gly Pro 20 25 30 Phe Leu Val Lys Thr Gly Tyr Ala Phe Val Asp Cys Pro Asp Glu Ser 35 40 45 Trp Ala Leu Lys Ala Ile Glu Ala Leu Ser Gly Lys Ile Glu Leu His 50 55 60 Gly Lys Pro Ile Glu Val Glu His Ser Val Pro Lys Arg Gln Arg Ile 65 70 75 80 Arg Lys Leu Gln Ile Arg Asn Ile Pro Pro His Leu Gln Trp Glu Val 85 90 95 Leu Asp Ser Leu Leu Val Gln Tyr Gly Val Val Glu Ser Cys Glu Gln 100 105 110 Val Asn Thr Asp Ser Glu Thr Ala Val Val Asn Val Thr Tyr Ser Ser 115 120 125 Lys Asp Gln Ala Arg Gln Ala Leu Asp Lys Leu Asn Gly Phe Gln Leu 130 135 140 Glu Asn Phe Thr Leu Lys Val Ala Tyr Ile Pro Asp Glu Thr Ala Ala 145 150 155 160 Gln Gln Asn Pro Leu Gln Gln Pro Arg Gly Arg Arg Gly Leu Gly Gln 165 170 175 Arg Gly Ser Ser Arg Gln Gly Ser Pro Gly Ser Val Ser Lys Gln Lys 180 185 190 Pro Cys Asp Leu Pro Leu Arg Leu Leu Val Pro Thr Gln Phe Val Gly 195 200 205 Ala Ile Ile Gly Lys Glu Gly Ala Thr Ile Arg Asn Ile Thr Lys Gln 210 215 220 Thr Gln Ser Lys Ile Asp Val His Arg Lys Glu Asn Ala Gly Ala Ala 225 230 235 240 Glu Lys Ser Ile Thr Ile Leu Ser Thr Pro Glu Gly Thr Ser Ala Ala 245 250 255 Cys Lys Ser Ile Leu Glu Ile Met His Lys Glu Ala Gln Asp Ile Lys 260 265 270 Phe Thr Glu Glu Ile Pro Leu Lys Ile Leu Ala His Asn Asn Phe Val 275 280 285 Gly Arg Leu Ile Gly Lys Glu Gly Arg Asn Leu Lys Lys Ile Glu Gln 290 295 300 Asp Thr Asp Thr Lys Ile Thr Ile Ser Pro Leu Gln Glu Leu Thr Leu 305 310 315 320 Tyr Asn Pro Glu Arg Thr Ile Thr Val Lys Gly Asn Val Glu Thr Cys 325 330 335 Ala Lys Ala Glu Glu Glu Ile Met Lys Lys Ile Arg Glu Ser Tyr Glu 340 345 350 Asn Asp Ile Ala Ser Met Asn Leu Gln Ala His Leu Ile Pro Gly Leu 355 360 365 Asn Leu Asn Ala Leu Gly Leu Phe Pro Pro Thr Ser Gly Met Pro Pro 370 375 380 Pro Thr Ser Gly Pro Pro Ser Ala Met Thr Pro Pro Tyr Pro Gln Phe 385 390 395 400 Glu Gln Ser Glu Thr Glu Thr Val His Leu Phe Ile Pro Ala Leu Ser 405 410 415 Val Gly Ala Ile Ile Gly Lys Gln Gly Gln His Ile Lys Gln Leu Ser 420 425 430 Arg Phe Ala Gly Ala Ser Ile Lys Ile Ala Pro Ala Glu Ala Pro Asp 435 440 445 Ala Lys Val Arg Met Val Ile Ile Thr Gly Pro Pro Glu Ala Gln Phe 450 455 460 Lys Ala Gln Gly Arg Ile Tyr Gly Lys Ile Lys Glu Glu Asn Phe Val 465 470 475 480 Ser Pro Lys Glu Glu Val Lys Leu Glu Ala His Ile Arg Val Pro Ser 485 490 495 Phe Ala Ala Gly Arg Val Ile Gly Lys Gly Gly Lys Thr Val Asn Glu 500 505 510 Leu Gln Asn Leu Ser Ser Ala Glu Val Val Val Pro Arg Asp Gln Thr 515 520 525 Pro Asp Glu Asn Asp Gln Val Val Val Lys Ile Thr Gly His Phe Tyr 530 535 540 Ala Cys Gln Val Ala Gln Arg Lys Ile Gln Glu Ile Leu Thr Gln Val 545 550 555 560 Lys Gln His Gln Gln Gln Lys Ala Leu Gln Ser Gly Pro Pro Gln Ser 565 570 575 Arg Arg Lys 349 207 DNA Homo sapiens 349 atgtggcagc ccctcttctt caagtggctc ttgtcctgtt gccctgggag ttctcaaatt 60 gctgcagcag cctccaccca gcctgaggat gacatcaata cacagaggaa gaagagtcag 120 gaaaagatga gagaagttac agactctcct gggcgacccc gagagcttac cattcctcag 180 acttcttcac atggtgctaa cagattt 207 350 69 PRT Homo sapiens 350 Met Trp Gln Pro Leu Phe Phe Lys Trp Leu Leu Ser Cys Cys Pro Gly 5 10 15 Ser Ser Gln Ile Ala Ala Ala Ala Ser Thr Gln Pro Glu Asp Asp Ile 20 25 30 Asn Thr Gln Arg Lys Lys Ser Gln Glu Lys Met Arg Glu Val Thr Asp 35 40 45 Ser Pro Gly Arg Pro Arg Glu Leu Thr Ile Pro Gln Thr Ser Ser His 50 55 60 Gly Ala Asn Arg Phe 65 351 1012 DNA Homo sapiens 351 ccctctagaa ataattttgt ttaactttaa gaaggagata tacatatgca tcaccatcac 60 catcacacgg ccgcgtccga taacttccag ctgtcccagg gtgggcaggg attcgccatt 120 ccgatcgggc aggcgatggc gatcgcgggc cagatcaagc ttcccaccgt tcatatcggg 180 cctaccgcct tcctcggctt gggtgttgtc gacaacaacg gcaacggcgc acgagtccaa 240 cgcgtggtcg ggagcgctcc ggcggcaagt ctcggcatct ccaccggcga cgtgatcacc 300 gcggtcgacg gcgctccgat caactcggcc accgcgatgg cggacgcgct taacgggcat 360 catcccggtg acgtcatctc ggtgacctgg caaaccaagt cgggcggcac gcgtacaggg 420 aacgtgacat tggccgaggg acccccggcc gaattcatgg attgggggac gctgcacact 480 ttcatcgggg gtgtcaacaa acactccacc agcatcggga aggtgtggat cacagtcatc 540 tttattttcc gagtcatgat cctcgtggtg gctgcccagg aagtgtgggg tgacgagcaa 600 gaggacttcg tctgcaacac actgcaaccg ggatgcaaaa atgtgtgcta tgaccacttt 660 ttcccggtgt cccacatccg gctgtgggcc ctccagctga tcttcgtctc caccccagcg 720 ctgctggtgg ccatgcatgt ggcctactac aggcacgaaa ccactcgcaa gttcaggcga 780 ggagagaaga ggaatgattt caaagacata gaggacatta aaaagcagaa ggttcggata 840 gaggggtgac tcgagcacca ccaccaccac cactgagatc cggctgctaa caaagcccga 900 aaggaagctg agttggctgc tgccaccgct gagcaataac tagcataacc ccttggggcc 960 tctaaacggg tcttgagggg ttttttgctg aaaggaggaa ctatatccgg at 1012 352 267 PRT Homo sapiens 352 Met His His His His His His Thr Ala Ala Ser Asp Asn Phe Gln Leu 5 10 15 Ser Gln Gly Gly Gln Gly Phe Ala Ile Pro Ile Gly Gln Ala Met Ala 20 25 30 Ile Ala Gly Gln Ile Lys Leu Pro Thr Val His Ile Gly Pro Thr Ala 35 40 45 Phe Leu Gly Leu Gly Val Val Asp Asn Asn Gly Asn Gly Ala Arg Val 50 55 60 Gln Arg Val Val Gly Ser Ala Pro Ala Ala Ser Leu Gly Ile Ser Thr 65 70 75 80 Gly Asp Val Ile Thr Ala Val Asp Gly Ala Pro Ile Asn Ser Ala Thr 85 90 95 Ala Met Ala Asp Ala Leu Asn Gly His His Pro Gly Asp Val Ile Ser 100 105 110 Val Thr Trp Gln Thr Lys Ser Gly Gly Thr Arg Thr Gly Asn Val Thr 115 120 125 Leu Ala Glu Gly Pro Pro Ala Glu Phe Met Asp Trp Gly Thr Leu His 130 135 140 Thr Phe Ile Gly Gly Val Asn Lys His Ser Thr Ser Ile Gly Lys Val 145 150 155 160 Trp Ile Thr Val Ile Phe Ile Phe Arg Val Met Ile Leu Val Val Ala 165 170 175 Ala Gln Glu Val Trp Gly Asp Glu Gln Glu Asp Phe Val Cys Asn Thr 180 185 190 Leu Gln Pro Gly Cys Lys Asn Val Cys Tyr Asp His Phe Phe Pro Val 195 200 205 Ser His Ile Arg Leu Trp Ala Leu Gln Leu Ile Phe Val Ser Thr Pro 210 215 220 Ala Leu Leu Val Ala Met His Val Ala Tyr Tyr Arg His Glu Thr Thr 225 230 235 240 Arg Lys Phe Arg Arg Gly Glu Lys Arg Asn Asp Phe Lys Asp Ile Glu 245 250 255 Asp Ile Lys Lys Gln Lys Val Arg Ile Glu Gly 260 265 353 900 DNA Homo sapiens 353 atgcatcacc atcaccatca cacggccgcg tccgataact tccagctgtc ccagggtggg 60 cagggattcg ccattccgat cgggcaggcg atggcgatcg cgggccagat caagcttccc 120 accgttcata tcgggcctac cgccttcctc ggcttgggtg ttgtcgacaa caacggcaac 180 ggcgcacgag tccaacgcgt ggtcgggagc gctccggcgg caagtctcgg catctccacc 240 ggcgacgtga tcaccgcggt cgacggcgct ccgatcaact cggccaccgc gatggcggac 300 gcgcttaacg ggcatcatcc cggtgacgtc atctcggtga cctggcaaac caagtcgggc 360 ggcacgcgta cagggaacgt gacattggcc gagggacccc cggccgaatt ccacgaaacc 420 actcgcaagt tcaggcgagg agagaagagg aatgatttca aagacataga ggacattaaa 480 aagcagaagg ttcggataga ggggtcgctg tggtggacgt acaccagcag catctttttc 540 cgaatcatct ttgaagcagc ctttatgtat gtgttttact tcctttacaa tgggtaccac 600 ctgccctggg tgttgaaatg tgggattgac ccctgcccca accttgttga ctgctttatt 660 tctaggccaa cagagaagac cgtgtttacc atttttatga tttctgcgtc tgtgatttgc 720 atgctgctta acgtggcaga gttgtgctac ctgctgctga aagtgtgttt taggagatca 780 aagagagcac agacgcaaaa aaatcacccc aatcatgccc taaaggagag taagcagaat 840 gaaatgaatg agctgatttc agatagtggt caaaatgcaa tcacaggttt cccaagctaa 900 354 299 PRT Homo sapiens 354 Met His His His His His His Thr Ala Ala Ser Asp Asn Phe Gln Leu 5 10 15 Ser Gln Gly Gly Gln Gly Phe Ala Ile Pro Ile Gly Gln Ala Met Ala 20 25 30 Ile Ala Gly Gln Ile Lys Leu Pro Thr Val His Ile Gly Pro Thr Ala 35 40 45 Phe Leu Gly Leu Gly Val Val Asp Asn Asn Gly Asn Gly Ala Arg Val 50 55 60 Gln Arg Val Val Gly Ser Ala Pro Ala Ala Ser Leu Gly Ile Ser Thr 65 70 75 80 Gly Asp Val Ile Thr Ala Val Asp Gly Ala Pro Ile Asn Ser Ala Thr 85 90 95 Ala Met Ala Asp Ala Leu Asn Gly His His Pro Gly Asp Val Ile Ser 100 105 110 Val Thr Trp Gln Thr Lys Ser Gly Gly Thr Arg Thr Gly Asn Val Thr 115 120 125 Leu Ala Glu Gly Pro Pro Ala Glu Phe His Glu Thr Thr Arg Lys Phe 130 135 140 Arg Arg Gly Glu Lys Arg Asn Asp Phe Lys Asp Ile Glu Asp Ile Lys 145 150 155 160 Lys Gln Lys Val Arg Ile Glu Gly Ser Leu Trp Trp Thr Tyr Thr Ser 165 170 175 Ser Ile Phe Phe Arg Ile Ile Phe Glu Ala Ala Phe Met Tyr Val Phe 180 185 190 Tyr Phe Leu Tyr Asn Gly Tyr His Leu Pro Trp Val Leu Lys Cys Gly 195 200 205 Ile Asp Pro Cys Pro Asn Leu Val Asp Cys Phe Ile Ser Arg Pro Thr 210 215 220 Glu Lys Thr Val Phe Thr Ile Phe Met Ile Ser Ala Ser Val Ile Cys 225 230 235 240 Met Leu Leu Asn Val Ala Glu Leu Cys Tyr Leu Leu Leu Lys Val Cys 245 250 255 Phe Arg Arg Ser Lys Arg Ala Gln Thr Gln Lys Asn His Pro Asn His 260 265 270 Ala Leu Lys Glu Ser Lys Gln Asn Glu Met Asn Glu Leu Ile Ser Asp 275 280 285 Ser Gly Gln Asn Ala Ile Thr Gly Phe Pro Ser 290 295 355 24 DNA Artificial Sequence Primer 355 ggagtacagc ttcaagacaa tggg 24 356 31 DNA Artificial Sequence Primer 356 ccatgggaat tcattataat aattttgttc c 31 357 920 PRT Homo sapiens 357 Met Gln His His His His His His Gly Val Gln Leu Gln Asp Asn Gly 1 5 10 15 Tyr Asn Gly Leu Leu Ile Ala Ile Asn Pro Gln Val Pro Glu Asn Gln 20 25 30 Asn Leu Ile Ser Asn Ile Lys Glu Met Ile Thr Glu Ala Ser Phe Tyr 35 40 45 Leu Phe Asn Ala Thr Lys Arg Arg Val Phe Phe Arg Asn Ile Lys Ile 50 55 60 Leu Ile Pro Ala Thr Trp Lys Ala Asn Asn Asn Ser Lys Ile Lys Gln 65 70 75 80 Glu Ser Tyr Glu Lys Ala Asn Val Ile Val Thr Asp Trp Tyr Gly Ala 85 90 95 His Gly Asp Asp Pro Tyr Thr Leu Gln Tyr Arg Gly Cys Gly Lys Glu 100 105 110 Gly Lys Tyr Ile His Phe Thr Pro Asn Phe Leu Leu Asn Asp Asn Leu 115 120 125 Thr Ala Gly Tyr Gly Ser Arg Gly Arg Val Phe Val His Glu Trp Ala 130 135 140 His Leu Arg Trp Gly Val Phe Asp Glu Tyr Asn Asn Asp Lys Pro Phe 145 150 155 160 Tyr Ile Asn Gly Gln Asn Gln Ile Lys Val Thr Arg Cys Ser Ser Asp 165 170 175 Ile Thr Gly Ile Phe Val Cys Glu Lys Gly Pro Cys Pro Gln Glu Asn 180 185 190 Cys Ile Ile Ser Lys Leu Phe Lys Glu Gly Cys Thr Phe Ile Tyr Asn 195 200 205 Ser Thr Gln Asn Ala Thr Ala Ser Ile Met Phe Met Gln Ser Leu Ser 210 215 220 Ser Val Val Glu Phe Cys Asn Ala Ser Thr His Asn Gln Glu Ala Pro 225 230 235 240 Asn Leu Gln Asn Gln Met Cys Ser Leu Arg Ser Ala Trp Asp Val Ile 245 250 255 Thr Asp Ser Ala Asp Phe His His Ser Phe Pro Met Asn Gly Thr Glu 260 265 270 Leu Pro Pro Pro Pro Thr Phe Ser Leu Val Glu Ala Gly Asp Lys Val 275 280 285 Val Cys Leu Val Leu Asp Val Ser Ser Lys Met Ala Glu Ala Asp Arg 290 295 300 Leu Leu Gln Leu Gln Gln Ala Ala Glu Phe Tyr Leu Met Gln Ile Val 305 310 315 320 Glu Ile His Thr Phe Val Gly Ile Ala Ser Phe Asp Ser Lys Gly Glu 325 330 335 Ile Arg Ala Gln Leu His Gln Ile Asn Ser Asn Asp Asp Arg Lys Leu 340 345 350 Leu Val Ser Tyr Leu Pro Thr Thr Val Ser Ala Lys Thr Asp Ile Ser 355 360 365 Ile Cys Ser Gly Leu Lys Lys Gly Phe Glu Val Val Glu Lys Leu Asn 370 375 380 Gly Lys Ala Tyr Gly Ser Val Met Ile Leu Val Thr Ser Gly Asp Asp 385 390 395 400 Lys Leu Leu Gly Asn Cys Leu Pro Thr Val Leu Ser Ser Gly Ser Thr 405 410 415 Ile His Ser Ile Ala Leu Gly Ser Ser Ala Ala Pro Asn Leu Glu Glu 420 425 430 Leu Ser Arg Leu Thr Gly Gly Leu Lys Phe Phe Val Pro Asp Ile Ser 435 440 445 Asn Ser Asn Ser Met Ile Asp Ala Phe Ser Arg Ile Ser Ser Gly Thr 450 455 460 Gly Asp Ile Phe Gln Gln His Ile Gln Leu Glu Ser Thr Gly Glu Asn 465 470 475 480 Val Lys Pro His His Gln Leu Lys Asn Thr Val Thr Val Asp Asn Thr 485 490 495 Val Gly Asn Asp Thr Met Phe Leu Val Thr Trp Gln Ala Ser Gly Pro 500 505 510 Pro Glu Ile Ile Leu Phe Asp Pro Asp Gly Arg Lys Tyr Tyr Thr Asn 515 520 525 Asn Phe Ile Thr Asn Leu Thr Phe Arg Thr Ala Ser Leu Trp Ile Pro 530 535 540 Gly Thr Ala Lys Pro Gly His Trp Thr Tyr Thr Leu Asn Asn Thr His 545 550 555 560 His Ser Leu Gln Ala Leu Lys Val Thr Val Thr Ser Arg Ala Ser Asn 565 570 575 Ser Ala Val Pro Pro Ala Thr Val Glu Ala Phe Val Glu Arg Asp Ser 580 585 590 Leu His Phe Pro His Pro Val Met Ile Tyr Ala Asn Val Lys Gln Gly 595 600 605 Phe Tyr Pro Ile Leu Asn Ala Thr Val Thr Ala Thr Val Glu Pro Glu 610 615 620 Thr Gly Asp Pro Val Thr Leu Arg Leu Leu Asp Asp Gly Ala Gly Ala 625 630 635 640 Asp Val Ile Lys Asn Asp Gly Ile Tyr Ser Arg Tyr Phe Phe Ser Phe 645 650 655 Ala Ala Asn Gly Arg Tyr Ser Leu Lys Val His Val Asn His Ser Pro 660 665 670 Ser Ile Ser Thr Pro Ala His Ser Ile Pro Gly Ser His Ala Met Tyr 675 680 685 Val Pro Gly Tyr Thr Ala Asn Gly Asn Ile Gln Met Asn Ala Pro Arg 690 695 700 Lys Ser Val Gly Arg Asn Glu Glu Glu Arg Lys Trp Gly Phe Ser Arg 705 710 715 720 Val Ser Ser Gly Gly Ser Phe Ser Val Leu Gly Val Pro Ala Gly Pro 725 730 735 His Pro Asp Val Phe Pro Pro Cys Lys Ile Ile Asp Leu Glu Ala Val 740 745 750 Lys Val Glu Glu Glu Leu Thr Leu Ser Trp Thr Ala Pro Gly Glu Asp 755 760 765 Phe Asp Gln Gly Gln Ala Thr Ser Tyr Glu Ile Arg Met Ser Lys Ser 770 775 780 Leu Gln Asn Ile Gln Asp Asp Phe Asn Asn Ala Ile Leu Val Asn Thr 785 790 795 800 Ser Lys Arg Asn Pro Gln Gln Ala Gly Ile Arg Glu Ile Phe Thr Phe 805 810 815 Ser Pro Gln Ile Ser Thr Asn Gly Pro Glu His Gln Pro Asn Gly Glu 820 825 830 Thr His Glu Ser His Arg Ile Tyr Val Ala Ile Arg Ala Met Asp Arg 835 840 845 Asn Ser Leu Gln Ser Ala Val Ser Asn Ile Ala Gln Ala Pro Leu Phe 850 855 860 Ile Pro Pro Asn Ser Asp Pro Val Pro Ala Arg Asp Tyr Leu Ile Leu 865 870 875 880 Lys Gly Val Leu Thr Ala Met Gly Leu Ile Gly Ile Ile Cys Leu Ile 885 890 895 Ile Val Val Thr His His Thr Leu Ser Arg Lys Lys Arg Ala Asp Lys 900 905 910 Lys Glu Asn Gly Thr Lys Leu Leu 915 920 358 2773 DNA Homo sapiens 358 catatgcagc atcaccacca tcaccacgga gtacagcttc aagacaatgg gtataatgga 60 ttgctcattg caattaatcc tcaggtacct gagaatcaga acctcatctc aaacattaag 120 gaaatgataa ctgaagcttc attttaccta tttaatgcta ccaagagaag agtatttttc 180 agaaatataa agattttaat acctgccaca tggaaagcta ataataacag caaaataaaa 240 caagaatcat atgaaaaggc aaatgtcata gtgactgact ggtatggggc acatggagat 300 gatccataca ccctacaata cagagggtgt ggaaaagagg gaaaatacat tcatttcaca 360 cctaatttcc tactgaatga taacttaaca gctggctacg gatcacgagg ccgagtgttt 420 gtccatgaat gggcccacct ccgttggggt gtgttcgatg agtataacaa tgacaaacct 480 ttctacataa atgggcaaaa tcaaattaaa gtgacaaggt gttcatctga catcacaggc 540 atttttgtgt gtgaaaaagg tccttgcccc caagaaaact gtattattag taagcttttt 600 aaagaaggat gcacctttat ctacaatagc acccaaaatg caactgcatc aataatgttc 660 atgcaaagtt tatcttctgt ggttgaattt tgtaatgcaa gtacccacaa ccaagaagca 720 ccaaacctac agaaccagat gtgcagcctc agaagtgcat gggatgtaat cacagactct 780 gctgactttc accacagctt tcccatgaac gggactgagc ttccacctcc tcccacattc 840 tcgcttgtag aggctggtga caaagtggtc tgtttagtgc tggatgtgtc cagcaagatg 900 gcagaggctg acagactcct tcaactacaa caagccgcag aattttattt gatgcagatt 960 gttgaaattc ataccttcgt gggcattgcc agtttcgaca gcaaaggaga gatcagagcc 1020 cagctacacc aaattaacag caatgatgat cgaaagttgc tggtttcata tctgcccacc 1080 actgtatcag ctaaaacaga catcagcatt tgttcagggc ttaagaaagg atttgaggtg 1140 gttgaaaaac tgaatggaaa agcttatggc tctgtgatga tattagtgac cagcggagat 1200 gataagcttc ttggcaattg cttacccact gtgctcagca gtggttcaac aattcactcc 1260 attgccctgg gttcatctgc agccccaaat ctggaggaat tatcacgtct tacaggaggt 1320 ttaaagttct ttgttccaga tatatcaaac tccaatagca tgattgatgc tttcagtaga 1380 atttcctctg gaactggaga cattttccag caacatattc agcttgaaag tacaggtgaa 1440 aatgtcaaac ctcaccatca attgaaaaac acagtgactg tggataatac tgtgggcaac 1500 gacactatgt ttctagttac gtggcaggcc agtggtcctc ctgagattat attatttgat 1560 cctgatggac gaaaatacta cacaaataat tttatcacca atctaacttt tcggacagct 1620 agtctttgga ttccaggaac agctaagcct gggcactgga cttacaccct gaacaatacc 1680 catcattctc tgcaagccct gaaagtgaca gtgacctctc gcgcctccaa ctcagctgtg 1740 cccccagcca ctgtggaagc ctttgtggaa agagacagcc tccattttcc tcatcctgtg 1800 atgatttatg ccaatgtgaa acagggattt tatcccattc ttaatgccac tgtcactgcc 1860 acagttgagc cagagactgg agatcctgtt acgctgagac tccttgatga tggagcaggt 1920 gctgatgtta taaaaaatga tggaatttac tcgaggtatt ttttctcctt tgctgcaaat 1980 ggtagatata gcttgaaagt gcatgtcaat cactctccca gcataagcac cccagcccac 2040 tctattccag ggagtcatgc tatgtatgta ccaggttaca cagcaaacgg taatattcag 2100 atgaatgctc caaggaaatc agtaggcaga aatgaggagg agcgaaagtg gggctttagc 2160 cgagtcagct caggaggctc cttttcagtg ctgggagttc cagctggccc ccaccctgat 2220 gtgtttccac catgcaaaat tattgacctg gaagctgtaa aagtagaaga ggaattgacc 2280 ctatcttgga cagcacctgg agaagacttt gatcagggcc aggctacaag ctatgaaata 2340 agaatgagta aaagtctaca gaatatccaa gatgacttta acaatgctat tttagtaaat 2400 acatcaaagc gaaatcctca gcaagctggc atcagggaga tatttacgtt ctcaccccaa 2460 atttccacga atggacctga acatcagcca aatggagaaa cacatgaaag ccacagaatt 2520 tatgttgcaa tacgagcaat ggataggaac tccttacagt ctgctgtatc taacattgcc 2580 caggcgcctc tgtttattcc ccccaattct gatcctgtac ctgccagaga ttatcttata 2640 ttgaaaggag ttttaacagc aatgggtttg ataggaatca tttgccttat tatagttgtg 2700 acacatcata ctttaagcag gaaaaagaga gcagacaaga aagagaatgg aacaaaatta 2760 ttataatgaa ttc 2773 359 25 DNA Artificial Sequence Primer 359 tggcagcccc tcttcttcaa gtggc 25 360 33 DNA Artificial Sequence Primer 360 cgccagaatt catcaaacaa atctgttagc acc 33 361 77 PRT Homo sapiens 361 Met Gln His His His His His His Trp Gln Pro Leu Phe Phe Lys Trp 1 5 10 15 Leu Leu Ser Cys Cys Pro Gly Ser Ser Gln Ile Ala Ala Ala Ala Ser 20 25 30 Thr Gln Pro Glu Asp Asp Ile Asn Thr Gln Arg Lys Lys Ser Gln Glu 35 40 45 Lys Met Arg Glu Val Thr Asp Ser Pro Gly Arg Pro Arg Glu Leu Thr 50 55 60 Ile Pro Gln Thr Ser Ser His Gly Ala Asn Arg Phe Val 65 70 75 362 244 DNA Homo sapiens 362 catatgcagc atcaccacca tcaccactgg cagcccctct tcttcaagtg gctcttgtcc 60 tgttgccctg ggagttctca aattgctgca gcagcctcca cccagcctga ggatgacatc 120 aatacacaga ggaagaagag tcaggaaaag atgagagaag ttacagactc tcctgggcga 180 ccccgagagc ttaccattcc tcagacttct tcacatggtg ctaacagatt tgtttgatga 240 attc 244 363 20 PRT Homo sapiens 363 Met Trp Gln Pro Leu Phe Phe Lys Trp Leu Leu Ser Cys Cys Pro Gly 5 10 15 Ser Ser Gln Ile 20 364 60 DNA Homo sapiens 364 atgtggcagc ccctcttctt caagtggctc ttgtcctgtt gccctgggag ttctcaaatt 60 365 20 PRT Homo sapiens 365 Gly Ser Ser Gln Ile Ala Ala Ala Ala Ser Thr Gln Pro Glu Asp Asp 5 10 15 Ile Asn Thr Gln 20 366 60 DNA Homo sapiens 366 gggagttctc aaattgctgc agcagcctcc acccagcctg aggatgacat caatacacag 60 367 20 PRT Homo sapiens 367 Lys Pro Gly His Trp Thr Tyr Thr Leu Asn Asn Thr His His Ser Leu 5 10 15 Gln Ala Leu Lys 20 368 2343 DNA Homo sapiens 368 attccggagc gtttgcggct tcgcttcatg gccgctctcc cgcccctcct gggatctgtg 60 gggagctggg gagcccgcag cggcccggag ccggagctgg cgagccgagc ggagacctgt 120 gcgccgcgcc tctgaggcgc agcatgtgaa gcggagacgg catccagtgg ggggcgagcc 180 tctcagccgg ccgggatggc taccacggcc gagctcttcg aggagccttt tgtggcagat 240 gaatatattg aacgtcttgt atggagaacc ccaggaggag gctctagagg tggacctgaa 300 gcttttgatc ctaaaagatt attagaagaa tttgtaaatc atattcagga actccagata 360 atggatgaaa ggattcagag gaaagtagag aaactagagc aacaatgtca gaaagaagcc 420 aaggaatttg ccaagaaggt acaagagctg cagaaaagca atcaggttgc cttccaacat 480 ttccaagaac tagatgagca cattagctat gtagcaacta aagtctgtca ccttggagac 540 cagttagagg gggtaaacac acccagacaa cgggcagtgg aggctcagaa attgatgaaa 600 tactttaatg agtttctaga tggagaattg aaatctgatg tttttacaaa ttctgaaaag 660 ataaaggaag cagcagacat cattcagaag ttgcacctaa ttgcccaaga gttacctttt 720 gatagatttt cagaagttaa atccaaaatt gcaagtaaat accatgattt agaatgccag 780 ctgattcagg agtttaccag tgctcaaaga agaggtgaaa tctccagaat gagagaagta 840 gcagcagttt tacttcattt taagggttat tcccattgtg ttgatgttta tataaagcag 900 tgccaggagg gtgcttattt gagaaatgat atatttgaag acgctggaat actctgtcaa 960 agagtgaaca aacaagttgg agatatcttc agtaatccag aaacagtcct ggctaaactt 1020 attcaaaatg tatttgaaat caaactacag agttttgtga aagagcagtt agaagaatgt 1080 aggaagtccg atgcagagca atatctcaaa aatctctatg atctgtatac aagaaccacc 1140 aatctttcca gcaagctgat ggagtttaat ttaggtactg ataaacagac tttcttgtct 1200 aagcttatca aatccatttt catttcctat ttggagaact atattgaggt ggagactgga 1260 tatttgaaaa gcagaagtgc tatgatccta cagcgctatt atgattcgaa aaaccatcaa 1320 aagagatcca ttggcacagg aggtattcaa gatttgaagg aaagaattag acagcgtacc 1380 aacttaccac ttgggccaag tatcgatact catggggaga cttttctatc ccaagaagtg 1440 gtggttaatc ttttacaaga aaccaaacaa gcctttgaaa gatgtcatag gctctctgat 1500 ccttctgact taccaaggaa tgccttcaga atttttacca ttcttgtgga atttttatgt 1560 attgagcata ttgattatgc tttggaaaca ggacttgctg gaattccctc ttcagattct 1620 aggaatgcaa atctttattt tttggacgtt gtgcaacagg ccaatactat ttttcatctt 1680 tttgacaaac agtttaatga tcaccttatg ccactaataa gctcttctcc taagttatct 1740 gaatgccttc agaagaaaaa agaaataatt gaacaaatgg agatgaaatt ggatactggc 1800 attgatagga cattaaattg tatgattgga cagatgaagc atattttggc tgcagaacag 1860 aagaaaacag attttaagcc agaagatgaa aacaatgttt tgattcaata tactaatgcc 1920 tgtgtaaaag tctgtgctta cgtaagaaaa caagtggaga agattaaaaa ttccatggat 1980 gggaagaatg tggatacagt tttgatggaa cttggagtac gttttcatcg acttatctat 2040 gagcatcttc aacaatattc ctacagttgt atgggtggca tgttggccat ttgtgatgta 2100 gccgaatata ggaagtgtgc caaagacttc aagattccaa tggtattaca tctttttgat 2160 actctgcatg ctctttgcaa tcttctggta gttgccccag ataatttaaa gcaagtctgc 2220 tcaggagaac aacttgctaa tctggacaag aatatacttc actccttcgt acaacttcgt 2280 gctgattata gatctgcccg ccttgctcga cacttcagct gagattgaat ttacaaagga 2340 att 2343 369 708 PRT Homo sapiens 369 Met Ala Thr Thr Ala Glu Leu Phe Glu Glu Pro Phe Val Ala Asp Glu 1 5 10 15 Tyr Ile Glu Arg Leu Val Trp Arg Thr Pro Gly Gly Gly Ser Arg Gly 20 25 30 Gly Pro Glu Ala Phe Asp Pro Lys Arg Leu Leu Glu Glu Phe Val Asn 35 40 45 His Ile Gln Glu Leu Gln Ile Met Asp Glu Arg Ile Gln Arg Lys Val 50 55 60 Glu Lys Leu Glu Gln Gln Cys Gln Lys Glu Ala Lys Glu Phe Ala Lys 65 70 75 80 Lys Val Gln Glu Leu Gln Lys Ser Asn Gln Val Ala Phe Gln His Phe 85 90 95 Gln Glu Leu Asp Glu His Ile Ser Tyr Val Ala Thr Lys Val Cys His 100 105 110 Leu Gly Asp Gln Leu Glu Gly Val Asn Thr Pro Arg Gln Arg Ala Val 115 120 125 Glu Ala Gln Lys Leu Met Lys Tyr Phe Asn Glu Phe Leu Asp Gly Glu 130 135 140 Leu Lys Ser Asp Val Phe Thr Asn Ser Glu Lys Ile Lys Glu Ala Ala 145 150 155 160 Asp Ile Ile Gln Lys Leu His Leu Ile Ala Gln Glu Leu Pro Phe Asp 165 170 175 Arg Phe Ser Glu Val Lys Ser Lys Ile Ala Ser Lys Tyr His Asp Leu 180 185 190 Glu Cys Gln Leu Ile Gln Glu Phe Thr Ser Ala Gln Arg Arg Gly Glu 195 200 205 Ile Ser Arg Met Arg Glu Val Ala Ala Val Leu Leu His Phe Lys Gly 210 215 220 Tyr Ser His Cys Val Asp Val Tyr Ile Lys Gln Cys Gln Glu Gly Ala 225 230 235 240 Tyr Leu Arg Asn Asp Ile Phe Glu Asp Ala Gly Ile Leu Cys Gln Arg 245 250 255 Val Asn Lys Gln Val Gly Asp Ile Phe Ser Asn Pro Glu Thr Val Leu 260 265 270 Ala Lys Leu Ile Gln Asn Val Phe Glu Ile Lys Leu Gln Ser Phe Val 275 280 285 Lys Glu Gln Leu Glu Glu Cys Arg Lys Ser Asp Ala Glu Gln Tyr Leu 290 295 300 Lys Asn Leu Tyr Asp Leu Tyr Thr Arg Thr Thr Asn Leu Ser Ser Lys 305 310 315 320 Leu Met Glu Phe Asn Leu Gly Thr Asp Lys Gln Thr Phe Leu Ser Lys 325 330 335 Leu Ile Lys Ser Ile Phe Ile Ser Tyr Leu Glu Asn Tyr Ile Glu Val 340 345 350 Glu Thr Gly Tyr Leu Lys Ser Arg Ser Ala Met Ile Leu Gln Arg Tyr 355 360 365 Tyr Asp Ser Lys Asn His Gln Lys Arg Ser Ile Gly Thr Gly Gly Ile 370 375 380 Gln Asp Leu Lys Glu Arg Ile Arg Gln Arg Thr Asn Leu Pro Leu Gly 385 390 395 400 Pro Ser Ile Asp Thr His Gly Glu Thr Phe Leu Ser Gln Glu Val Val 405 410 415 Val Asn Leu Leu Gln Glu Thr Lys Gln Ala Phe Glu Arg Cys His Arg 420 425 430 Leu Ser Asp Pro Ser Asp Leu Pro Arg Asn Ala Phe Arg Ile Phe Thr 435 440 445 Ile Leu Val Glu Phe Leu Cys Ile Glu His Ile Asp Tyr Ala Leu Glu 450 455 460 Thr Gly Leu Ala Gly Ile Pro Ser Ser Asp Ser Arg Asn Ala Asn Leu 465 470 475 480 Tyr Phe Leu Asp Val Val Gln Gln Ala Asn Thr Ile Phe His Leu Phe 485 490 495 Asp Lys Gln Phe Asn Asp His Leu Met Pro Leu Ile Ser Ser Ser Pro 500 505 510 Lys Leu Ser Glu Cys Leu Gln Lys Lys Lys Glu Ile Ile Glu Gln Met 515 520 525 Glu Met Lys Leu Asp Thr Gly Ile Asp Arg Thr Leu Asn Cys Met Ile 530 535 540 Gly Gln Met Lys His Ile Leu Ala Ala Glu Gln Lys Lys Thr Asp Phe 545 550 555 560 Lys Pro Glu Asp Glu Asn Asn Val Leu Ile Gln Tyr Thr Asn Ala Cys 565 570 575 Val Lys Val Cys Ala Tyr Val Arg Lys Gln Val Glu Lys Ile Lys Asn 580 585 590 Ser Met Asp Gly Lys Asn Val Asp Thr Val Leu Met Glu Leu Gly Val 595 600 605 Arg Phe His Arg Leu Ile Tyr Glu His Leu Gln Gln Tyr Ser Tyr Ser 610 615 620 Cys Met Gly Gly Met Leu Ala Ile Cys Asp Val Ala Glu Tyr Arg Lys 625 630 635 640 Cys Ala Lys Asp Phe Lys Ile Pro Met Val Leu His Leu Phe Asp Thr 645 650 655 Leu His Ala Leu Cys Asn Leu Leu Val Val Ala Pro Asp Asn Leu Lys 660 665 670 Gln Val Cys Ser Gly Glu Gln Leu Ala Asn Leu Asp Lys Asn Ile Leu 675 680 685 His Ser Phe Val Gln Leu Arg Ala Asp Tyr Arg Ser Ala Arg Leu Ala 690 695 700 Arg His Phe Ser 705 370 60 DNA Homo sapiens 370 gtcaatcact ctcccagcat aagcacccca gcccactcta ttccagggag tcatgctatg 60 371 60 DNA Homo sapiens 371 agtagaattt cctctggaac tggagacatt ttccagcaac atattcagct tgaaagtaca 60 372 60 DNA Homo sapiens 372 ccagagactg gagatcctgt tacgctgaga ctccttgatg atggagcagg tgctgatgtt 60 373 60 DNA Homo sapiens 373 ttacagtctg ctgtatctaa cattgcccag gcgcctctgt ttattccccc caattctgat 60 374 60 DNA Homo sapiens 374 gctgtgcccc cagccactgt ggaagccttt gtggaaagag acagcctcca ttttcctcat 60 375 60 DNA Homo sapiens 375 aaaaacacag tgactgtgga taatactgtg ggcaacgaca ctatgtttct agttacgtgg 60 376 20 PRT Homo sapiens 376 Leu Gln Ser Ala Val Ser Asn Ile Ala Gln Ala Pro Leu Phe Ile Pro 5 10 15 Pro Asn Ser Asp 20 377 20 PRT Homo sapiens 377 Val Asn His Ser Pro Ser Ile Ser Thr Pro Ala His Ser Ile Pro Gly 5 10 15 Ser His Ala Met 20 378 20 PRT Homo sapiens 378 Pro Glu Thr Gly Asp Pro Val Thr Leu Arg Leu Leu Asp Asp Gly Ala 5 10 15 Gly Ala Asp Val 20 379 20 PRT Homo sapiens 379 Ala Val Pro Pro Ala Thr Val Glu Ala Phe Val Glu Arg Asp Ser Leu 5 10 15 His Phe Pro His 20 380 20 PRT Homo sapiens 380 Ser Arg Ile Ser Ser Gly Thr Gly Asp Ile Phe Gln Gln His Ile Gln 5 10 15 Leu Glu Ser Thr 20 381 20 PRT Homo sapiens 381 Lys Asn Thr Val Thr Val Asp Asn Thr Val Gly Asn Asp Thr Met Phe 5 10 15 Leu Val Thr Trp 20 382 20 PRT Homo sapiens 382 Lys Pro Gly His Trp Thr Tyr Thr Leu Asn Asn Thr His His Ser Leu 1 5 10 15 Gln Ala Leu Lys 20 383 29 DNA Artificial Sequence PCR primer 383 cggcgaattc atggattggg ggacgctgc 29 384 35 DNA Artificial Sequence PCR primer 384 cggcctcgag tcacccctct atccgaacct tctgc 35 385 32 DNA Artificial Sequence PCR primer 385 cggcgaattc cacgaaccac tcgcaagttc ag 32 386 30 DNA Artificial Sequence PCR primer 386 cggctcgagt tagcttgggc ctgtgattgc 30 387 20 PRT Homo sapiens 387 Phe Phe Lys Trp Leu Leu Ser Cys Cys Pro Gly Ser Ser Gln Ile Ala 1 5 10 15 Ala Ala Ala Ser 20 388 19 PRT Homo sapiens 388 Leu Ser Cys Cys Pro Gly Ser Ser Gln Ile Ala Ala Ala Ser Thr Gln 1 5 10 15 Pro Glu Asp 389 20 PRT Homo sapiens 389 Ala Ala Ala Ala Ser Thr Gln Pro Glu Asp Asp Ile Asn Thr Gln Arg 1 5 10 15 Lys Lys Ser Gln 20 390 20 PRT Homo sapiens 390 Thr Gln Pro Glu Asp Asp Ile Asn Thr Gln Arg Lys Lys Ser Gln Glu 1 5 10 15 Lys Met Arg Glu 20 391 20 PRT Homo sapiens 391 Asp Ile Asn Thr Gln Arg Lys Lys Ser Gln Glu Lys Met Arg Glu Val 1 5 10 15 Thr Asp Ser Pro 20 392 20 PRT Homo sapiens 392 Arg Lys Lys Ser Gln Glu Lys Met Arg Glu Val Thr Asp Ser Pro Gly 1 5 10 15 Arg Pro Arg Glu 20 393 20 PRT Homo sapiens 393 Glu Lys Met Arg Glu Val Thr Asp Ser Pro Gly Arg Pro Arg Glu Leu 1 5 10 15 Thr Ile Pro Gln 20 394 20 PRT Homo sapiens 394 Val Thr Asp Ser Pro Gly Arg Pro Arg Glu Leu Thr Ile Pro Gln Thr 1 5 10 15 Ser Ser His Gly 20 395 19 PRT Homo sapiens 395 Gly Arg Pro Arg Glu Leu Thr Ile Pro Gln Thr Ser Ser His Gly Ala 1 5 10 15 Asn Arg Phe 396 19 PRT Homo sapiens 396 Met Asn Lys Leu Tyr Ile Gly Asn Leu Ser Glu Asn Ala Ala Pro Ser 5 10 15 Asp Leu Glu 397 20 PRT Homo sapiens 397 Ser Glu Asn Ala Ala Pro Ser Asp Leu Glu Ser Ile Phe Lys Asp Ala 5 10 15 Lys Ile Pro Val 20 398 20 PRT Homo sapiens 398 Ser Ile Phe Lys Asp Ala Lys Ile Pro Val Ser Gly Pro Phe Leu Val 5 10 15 Lys Thr Gly Tyr 20 399 20 PRT Homo sapiens 399 Ser Gly Pro Phe Leu Val Lys Thr Gly Tyr Ala Phe Val Asp Cys Pro 5 10 15 Asp Glu Ser Trp 20 400 20 PRT Homo sapiens 400 Ala Phe Val Asp Cys Pro Asp Glu Ser Trp Ala Leu Lys Ala Ile Glu 5 10 15 Ala Leu Ser Gly 20 401 20 PRT Homo sapiens 401 Ala Leu Lys Ala Ile Glu Ala Leu Ser Gly Lys Ile Glu Leu His Gly 5 10 15 Lys Pro Ile Glu 20 402 20 PRT Homo sapiens 402 Lys Ile Glu Leu His Gly Lys Pro Ile Glu Val Glu His Ser Val Pro 5 10 15 Lys Arg Gln Arg 20 403 20 PRT Homo sapiens 403 Val Glu His Ser Val Pro Lys Arg Gln Arg Ile Arg Lys Leu Gln Ile 5 10 15 Arg Asn Ile Pro 20 404 20 PRT Homo sapiens 404 Ile Arg Lys Leu Gln Ile Arg Asn Ile Pro Pro His Leu Gln Trp Glu 5 10 15 Val Leu Asp Ser 20 405 20 PRT Homo sapiens 405 Ala Val Val Asn Val Thr Tyr Ser Ser Lys Asp Gln Ala Arg Gln Ala 5 10 15 Leu Asp Lys Leu 20 406 20 PRT Homo sapiens 406 Asp Gln Ala Arg Gln Ala Leu Asp Lys Leu Asn Gly Phe Gln Leu Glu 5 10 15 Asn Phe Thr Leu 20 407 20 PRT Homo sapiens 407 Asn Gly Phe Gln Leu Glu Asn Phe Thr Leu Lys Val Ala Tyr Ile Pro 5 10 15 Asp Glu Thr Ala 20 408 20 PRT Homo sapiens 408 Lys Val Ala Tyr Ile Pro Asp Glu Thr Ala Ala Gln Gln Asn Pro Leu 5 10 15 Gln Gln Pro Arg 20 409 20 PRT Homo sapiens 409 Ala Gln Gln Asn Pro Leu Gln Gln Pro Arg Gly Arg Arg Gly Leu Gly 5 10 15 Gln Arg Gly Ser 20 410 20 PRT Homo sapiens 410 Gly Arg Arg Gly Leu Gly Gln Arg Gly Ser Ser Arg Gln Gly Ser Pro 5 10 15 Gly Ser Val Ser 20 411 20 PRT Homo sapiens 411 Ser Arg Gln Gly Ser Pro Gly Ser Val Ser Lys Gln Lys Pro Cys Asp 5 10 15 Leu Pro Leu Arg 20 412 20 PRT Homo sapiens 412 Lys Gln Lys Pro Cys Asp Leu Pro Leu Arg Leu Leu Val Pro Thr Gln 5 10 15 Phe Val Gly Ala 20 413 20 PRT Homo sapiens 413 Leu Leu Val Pro Thr Gln Phe Val Gly Ala Ile Ile Gly Lys Glu Gly 5 10 15 Ala Thr Ile Arg 20 414 20 PRT Homo sapiens 414 Ile Ile Gly Lys Glu Gly Ala Thr Ile Arg Asn Ile Thr Lys Gln Thr 5 10 15 Gln Ser Lys Ile 20 415 20 PRT Homo sapiens 415 Asn Ile Thr Lys Gln Thr Gln Ser Lys Ile Asp Val His Arg Lys Glu 5 10 15 Asn Ala Gly Ala 20 416 20 PRT Homo sapiens 416 Asp Val His Arg Lys Glu Asn Ala Gly Ala Ala Glu Lys Ser Ile Thr 5 10 15 Ile Leu Ser Thr 20 417 20 PRT Homo sapiens 417 Ala Glu Lys Ser Ile Thr Ile Leu Ser Thr Pro Glu Gly Thr Ser Ala 5 10 15 Ala Cys Lys Ser 20 418 20 PRT Homo sapiens 418 Pro Glu Gly Thr Ser Ala Ala Cys Lys Ser Ile Leu Glu Ile Met His 5 10 15 Lys Glu Ala Gln 20 419 20 PRT Homo sapiens 419 Ile Leu Glu Ile Met His Lys Glu Ala Gln Asp Ile Lys Phe Thr Glu 5 10 15 Glu Ile Pro Leu 20 420 455 DNA Homo sapiens 420 gaagacatgc ttacttcccc ttcaccttcc ttcatgatgt gggaagagtg ctgcaaccca 60 gccctagcca acgccgcatg agagggagtg tgccgagggc ttctgagaag gtttctctca 120 catctagaaa gaagcgctta agatgtggca gcccctcttc ttcaagtggc tcttgtcctg 180 ttgccctggg agttctcaaa ttgctgcagc agcctccacc cagcctgagg atgacatcaa 240 tacacagagg aagaagagtc aggaaaagat gagagaagtt acagactctc ctgggcgacc 300 ccgagagctt accattcctc agacttcttc acatggtgct aacagatttg ttcctaaaag 360 taaagctcta gaggccgtca aattggcaat agaagccggg ttccaccata ttgattctgc 420 acatgtttac aataatgagg agcaggttgg actgg 455 421 24 DNA Artificial Sequence Primer 421 actagtgtcc gcgtggcggc ctac 24 422 34 DNA Artificial Sequence Primer 422 catgagaatt catcacatgc ccttgaaggc tccc 34 423 161 PRT Homo sapiens 423 Met Gln His His His His His His His Thr Ser Val Arg Val Ala Ala 1 5 10 15 Tyr Phe Glu Asn Phe Leu Ala Ala Trp Arg Pro Val Lys Ala Ser Asp 20 25 30 Gly Asp Tyr Tyr Thr Leu Ala Val Pro Met Gly Asp Val Pro Met Asp 35 40 45 Gly Ile Ser Val Ala Asp Ile Gly Ala Ala Val Ser Ser Ile Phe Asn 50 55 60 Ser Pro Glu Glu Phe Leu Gly Lys Ala Val Gly Leu Ser Ala Glu Ala 65 70 75 80 Leu Thr Ile Gln Gln Tyr Ala Asp Val Leu Ser Lys Ala Leu Gly Lys 85 90 95 Glu Val Arg Asp Ala Lys Ile Thr Pro Glu Ala Phe Glu Lys Leu Gly 100 105 110 Phe Pro Ala Ala Lys Glu Ile Ala Asn Met Cys Arg Phe Tyr Glu Met 115 120 125 Lys Pro Asp Arg Asp Val Asn Leu Thr His Gln Leu Asn Pro Lys Val 130 135 140 Lys Ser Phe Ser Gln Phe Ile Ser Glu Asn Gln Gly Ala Phe Lys Gly 145 150 155 160 Met 424 489 DNA Homo sapiens 424 atgcagcatc accaccatca ccaccacact agtgtccgcg tggcggccta ctttgaaaac 60 tttctcgcgg cgtggcggcc cgtgaaagcc tctgatggag attactacac cttggctgta 120 ccgatgggag atgtaccaat ggatggtatc tctgttgctg atattggagc agccgtctct 180 agcattttta attctccaga ggaattttta ggcaaggccg tggggctcag tgcagaagca 240 ctaacaatac agcaatatgc tgatgttttg tccaaggctt tggggaaaga agtccgagat 300 gcaaagatta ccccggaagc tttcgagaag ctgggattcc ctgcagcaaa ggaaatagcc 360 aatatgtgtc gtttctatga aatgaagcca gaccgagatg tcaatctcac ccaccaacta 420 aatcccaaag tcaaaagctt cagccagttt atctcagaga accagggagc cttcaagggc 480 atgtgatga 489 425 32 DNA Artificial Sequence Primer 425 aacaaactgt atatcggaaa cctcagcgag aa 32 426 33 DNA Artificial Sequence Primer 426 ccatagaatt cattacttcc gtcttgactg agg 33 427 586 PRT Homo sapiens 427 Met Gln His His His His His His Asn Lys Leu Tyr Ile Gly Asn Leu 1 5 10 15 Ser Glu Asn Ala Ala Pro Ser Asp Leu Glu Ser Ile Phe Lys Asp Ala 20 25 30 Lys Ile Pro Val Ser Gly Pro Phe Leu Val Lys Thr Gly Tyr Ala Phe 35 40 45 Val Asp Cys Pro Asp Glu Ser Trp Ala Leu Lys Ala Ile Glu Ala Leu 50 55 60 Ser Gly Lys Ile Glu Leu His Gly Lys Pro Ile Glu Val Glu His Ser 65 70 75 80 Val Pro Lys Arg Gln Arg Ile Arg Lys Leu Gln Ile Arg Asn Ile Pro 85 90 95 Pro His Leu Gln Trp Glu Val Leu Asp Ser Leu Leu Val Gln Tyr Gly 100 105 110 Val Val Glu Ser Cys Glu Gln Val Asn Thr Asp Ser Glu Thr Ala Val 115 120 125 Val Asn Val Thr Tyr Ser Ser Lys Asp Gln Ala Arg Gln Ala Leu Asp 130 135 140 Lys Leu Asn Gly Phe Gln Leu Glu Asn Phe Thr Leu Lys Val Ala Tyr 145 150 155 160 Ile Pro Asp Glu Thr Ala Ala Gln Gln Asn Pro Leu Gln Gln Pro Arg 165 170 175 Gly Arg Arg Gly Leu Gly Gln Arg Gly Ser Ser Arg Gln Gly Ser Pro 180 185 190 Gly Ser Val Ser Lys Gln Lys Pro Cys Asp Leu Pro Leu Arg Leu Leu 195 200 205 Val Pro Thr Gln Phe Val Gly Ala Ile Ile Gly Lys Glu Gly Ala Thr 210 215 220 Ile Arg Asn Ile Thr Lys Gln Thr Gln Ser Lys Ile Asp Val His Arg 225 230 235 240 Lys Glu Asn Ala Gly Ala Ala Glu Lys Ser Ile Thr Ile Leu Ser Thr 245 250 255 Pro Glu Gly Thr Ser Ala Ala Cys Lys Ser Ile Leu Glu Ile Met His 260 265 270 Lys Glu Ala Gln Asp Ile Lys Phe Thr Glu Glu Ile Pro Leu Lys Ile 275 280 285 Leu Ala His Asn Asn Phe Val Gly Arg Leu Ile Gly Lys Glu Gly Arg 290 295 300 Asn Leu Lys Lys Ile Glu Gln Asp Thr Asp Thr Lys Ile Thr Ile Ser 305 310 315 320 Pro Leu Gln Glu Leu Thr Leu Tyr Asn Pro Glu Arg Thr Ile Thr Val 325 330 335 Lys Gly Asn Val Glu Thr Cys Ala Lys Ala Glu Glu Glu Ile Met Lys 340 345 350 Lys Ile Arg Glu Ser Tyr Glu Asn Asp Ile Ala Ser Met Asn Leu Gln 355 360 365 Ala His Leu Ile Pro Gly Leu Asn Leu Asn Ala Leu Gly Leu Phe Pro 370 375 380 Pro Thr Ser Gly Met Pro Pro Pro Thr Ser Gly Pro Pro Ser Ala Met 385 390 395 400 Thr Pro Pro Tyr Pro Gln Phe Glu Gln Ser Glu Thr Glu Thr Val His 405 410 415 Leu Phe Ile Pro Ala Leu Ser Val Gly Ala Ile Ile Gly Lys Gln Gly 420 425 430 Gln His Ile Lys Gln Leu Ser Arg Phe Ala Gly Ala Ser Ile Lys Ile 435 440 445 Ala Pro Ala Glu Ala Pro Asp Ala Lys Val Arg Met Val Ile Ile Thr 450 455 460 Gly Pro Pro Glu Ala Gln Phe Lys Ala Gln Gly Arg Ile Tyr Gly Lys 465 470 475 480 Ile Lys Glu Glu Asn Phe Val Ser Pro Lys Glu Glu Val Lys Leu Glu 485 490 495 Ala His Ile Arg Val Pro Ser Phe Ala Ala Gly Arg Val Ile Gly Lys 500 505 510 Gly Gly Lys Thr Val Asn Glu Leu Gln Asn Leu Ser Ser Ala Glu Val 515 520 525 Val Val Pro Arg Asp Gln Thr Pro Asp Glu Asn Asp Gln Val Val Val 530 535 540 Lys Ile Thr Gly His Phe Tyr Ala Cys Gln Val Ala Gln Arg Lys Ile 545 550 555 560 Gln Glu Ile Leu Thr Gln Val Lys Gln His Gln Gln Gln Lys Ala Leu 565 570 575 Gln Ser Gly Pro Pro Gln Ser Arg Arg Lys 580 585 428 1764 DNA Homo sapiens 428 atgcagcatc accaccatca ccacaacaaa ctgtatatcg gaaacctcag cgagaacgcc 60 gccccctcgg acctagaaag tatcttcaag gacgccaaga tcccggtgtc gggacccttc 120 ctggtgaaga ctggctacgc gttcgtggac tgcccggacg agagctgggc cctcaaggcc 180 atcgaggcgc tttcaggtaa aatagaactg cacgggaaac ccatagaagt tgagcactcg 240 gtcccaaaaa ggcaaaggat tcggaaactt cagatacgaa atatcccgcc tcatttacag 300 tgggaggtgc tggatagttt actagtccag tatggagtgg tggagagctg tgagcaagtg 360 aacactgact cggaaactgc agttgtaaat gtaacctatt ccagtaagga ccaagctaga 420 caagcactag acaaactgaa tggatttcag ttagagaatt tcaccttgaa agtagcctat 480 atccctgatg aaacggccgc ccagcaaaac cccttgcagc agccccgagg tcgccggggg 540 cttgggcaga ggggctcctc aaggcagggg tctccaggat ccgtatccaa gcagaaacca 600 tgtgatttgc ctctgcgcct gctggttccc acccaatttg ttggagccat cataggaaaa 660 gaaggtgcca ccattcggaa catcaccaaa cagacccagt ctaaaatcga tgtccaccgt 720 aaagaaaatg cgggggctgc tgagaagtcg attactatcc tctctactcc tgaaggcacc 780 tctgcggctt gtaagtctat tctggagatt atgcataagg aagctcaaga tataaaattc 840 acagaagaga tccccttgaa gattttagct cataataact ttgttggacg tcttattggt 900 aaagaaggaa gaaatcttaa aaaaattgag caagacacag acactaaaat cacgatatct 960 ccattgcagg aattgacgct gtataatcca gaacgcacta ttacagttaa aggcaatgtt 1020 gagacatgtg ccaaagctga ggaggagatc atgaagaaaa tcagggagtc ttatgaaaat 1080 gatattgctt ctatgaatct tcaagcacat ttaattcctg gattaaatct gaacgccttg 1140 ggtctgttcc cacccacttc agggatgcca cctcccacct cagggccccc ttcagccatg 1200 actcctccct acccgcagtt tgagcaatca gaaacggaga ctgttcatct gtttatccca 1260 gctctatcag tcggtgccat catcggcaag cagggccagc acatcaagca gctttctcgc 1320 tttgctggag cttcaattaa gattgctcca gcggaagcac cagatgctaa agtgaggatg 1380 gtgattatca ctggaccacc agaggctcag ttcaaggctc agggaagaat ttatggaaaa 1440 attaaagaag aaaactttgt tagtcctaaa gaagaggtga aacttgaagc tcatatcaga 1500 gtgccatcct ttgctgctgg cagagttatt ggaaaaggag gcaaaacggt gaatgaactt 1560 cagaatttgt caagtgcaga agttgttgtc cctcgtgacc agacacctga tgagaatgac 1620 caagtggttg tcaaaataac tggtcacttc tatgcttgcc aggttgccca gagaaaaatt 1680 caggaaattc tgactcaggt aaagcagcac caacaacaga aggctctgca aagtggacca 1740 cctcagtcaa gacggaagta atga 1764 429 35 DNA Artificial Sequence Primer 429 ccatggaatt cattatttca atataagata atctc 35 430 881 PRT Homo sapiens 430 Met Gln His His His His His His Gly Val Gln Leu Gln Asp Asn Gly 1 5 10 15 Tyr Asn Gly Leu Leu Ile Ala Ile Asn Pro Gln Val Pro Glu Asn Gln 20 25 30 Asn Leu Ile Ser Asn Ile Lys Glu Met Ile Thr Glu Ala Ser Phe Tyr 35 40 45 Leu Phe Asn Ala Thr Lys Arg Arg Val Phe Phe Arg Asn Ile Lys Ile 50 55 60 Leu Ile Pro Ala Thr Trp Lys Ala Asn Asn Asn Ser Lys Ile Lys Gln 65 70 75 80 Glu Ser Tyr Glu Lys Ala Asn Val Ile Val Thr Asp Trp Tyr Gly Ala 85 90 95 His Gly Asp Asp Pro Tyr Thr Leu Gln Tyr Arg Gly Cys Gly Lys Glu 100 105 110 Gly Lys Tyr Ile His Phe Thr Pro Asn Phe Leu Leu Asn Asp Asn Leu 115 120 125 Thr Ala Gly Tyr Gly Ser Arg Gly Arg Val Phe Val His Glu Trp Ala 130 135 140 His Leu Arg Trp Gly Val Phe Asp Glu Tyr Asn Asn Asp Lys Pro Phe 145 150 155 160 Tyr Ile Asn Gly Gln Asn Gln Ile Lys Val Thr Arg Cys Ser Ser Asp 165 170 175 Ile Thr Gly Ile Phe Val Cys Glu Lys Gly Pro Cys Pro Gln Glu Asn 180 185 190 Cys Ile Ile Ser Lys Leu Phe Lys Glu Gly Cys Thr Phe Ile Tyr Asn 195 200 205 Ser Thr Gln Asn Ala Thr Ala Ser Ile Met Phe Met Gln Ser Leu Ser 210 215 220 Ser Val Val Glu Phe Cys Asn Ala Ser Thr His Asn Gln Glu Ala Pro 225 230 235 240 Asn Leu Gln Asn Gln Met Cys Ser Leu Arg Ser Ala Trp Asp Val Ile 245 250 255 Thr Asp Ser Ala Asp Phe His His Ser Phe Pro Met Asn Gly Thr Glu 260 265 270 Leu Pro Pro Pro Pro Thr Phe Ser Leu Val Glu Ala Gly Asp Lys Val 275 280 285 Val Cys Leu Val Leu Asp Val Ser Ser Lys Met Ala Glu Ala Asp Arg 290 295 300 Leu Leu Gln Leu Gln Gln Ala Ala Glu Phe Tyr Leu Met Gln Ile Val 305 310 315 320 Glu Ile His Thr Phe Val Gly Ile Ala Ser Phe Asp Ser Lys Gly Glu 325 330 335 Ile Arg Ala Gln Leu His Gln Ile Asn Ser Asn Asp Asp Arg Lys Leu 340 345 350 Leu Val Ser Tyr Leu Pro Thr Thr Val Ser Ala Lys Thr Asp Ile Ser 355 360 365 Ile Cys Ser Gly Leu Lys Lys Gly Phe Glu Val Val Glu Lys Leu Asn 370 375 380 Gly Lys Ala Tyr Gly Ser Val Met Ile Leu Val Thr Ser Gly Asp Asp 385 390 395 400 Lys Leu Leu Gly Asn Cys Leu Pro Thr Val Leu Ser Ser Gly Ser Thr 405 410 415 Ile His Ser Ile Ala Leu Gly Ser Ser Ala Ala Pro Asn Leu Glu Glu 420 425 430 Leu Ser Arg Leu Thr Gly Gly Leu Lys Phe Phe Val Pro Asp Ile Ser 435 440 445 Asn Ser Asn Ser Met Ile Asp Ala Phe Ser Arg Ile Ser Ser Gly Thr 450 455 460 Gly Asp Ile Phe Gln Gln His Ile Gln Leu Glu Ser Thr Gly Glu Asn 465 470 475 480 Val Lys Pro His His Gln Leu Lys Asn Thr Val Thr Val Asp Asn Thr 485 490 495 Val Gly Asn Asp Thr Met Phe Leu Val Thr Trp Gln Ala Ser Gly Pro 500 505 510 Pro Glu Ile Ile Leu Phe Asp Pro Asp Gly Arg Lys Tyr Tyr Thr Asn 515 520 525 Asn Phe Ile Thr Asn Leu Thr Phe Arg Thr Ala Ser Leu Trp Ile Pro 530 535 540 Gly Thr Ala Lys Pro Gly His Trp Thr Tyr Thr Leu Asn Asn Thr His 545 550 555 560 His Ser Leu Gln Ala Leu Lys Val Thr Val Thr Ser Arg Ala Ser Asn 565 570 575 Ser Ala Val Pro Pro Ala Thr Val Glu Ala Phe Val Glu Arg Asp Ser 580 585 590 Leu His Phe Pro His Pro Val Met Ile Tyr Ala Asn Val Lys Gln Gly 595 600 605 Phe Tyr Pro Ile Leu Asn Ala Thr Val Thr Ala Thr Val Glu Pro Glu 610 615 620 Thr Gly Asp Pro Val Thr Leu Arg Leu Leu Asp Asp Gly Ala Gly Ala 625 630 635 640 Asp Val Ile Lys Asn Asp Gly Ile Tyr Ser Arg Tyr Phe Phe Ser Phe 645 650 655 Ala Ala Asn Gly Arg Tyr Ser Leu Lys Val His Val Asn His Ser Pro 660 665 670 Ser Ile Ser Thr Pro Ala His Ser Ile Pro Gly Ser His Ala Met Tyr 675 680 685 Val Pro Gly Tyr Thr Ala Asn Gly Asn Ile Gln Met Asn Ala Pro Arg 690 695 700 Lys Ser Val Gly Arg Asn Glu Glu Glu Arg Lys Trp Gly Phe Ser Arg 705 710 715 720 Val Ser Ser Gly Gly Ser Phe Ser Val Leu Gly Val Pro Ala Gly Pro 725 730 735 His Pro Asp Val Phe Pro Pro Cys Lys Ile Ile Asp Leu Glu Ala Val 740 745 750 Lys Val Glu Glu Glu Leu Thr Leu Ser Trp Thr Ala Pro Gly Glu Asp 755 760 765 Phe Asp Gln Gly Gln Ala Thr Ser Tyr Glu Ile Arg Met Ser Lys Ser 770 775 780 Leu Gln Asn Ile Gln Asp Asp Phe Asn Asn Ala Ile Leu Val Asn Thr 785 790 795 800 Ser Lys Arg Asn Pro Gln Gln Ala Gly Ile Arg Glu Ile Phe Thr Phe 805 810 815 Ser Pro Gln Ile Ser Thr Asn Gly Pro Glu His Gln Pro Asn Gly Glu 820 825 830 Thr His Glu Ser His Arg Ile Tyr Val Ala Ile Arg Ala Met Asp Arg 835 840 845 Asn Ser Leu Gln Ser Ala Val Ser Asn Ile Ala Gln Ala Pro Leu Phe 850 855 860 Ile Pro Pro Asn Ser Asp Pro Val Pro Ala Arg Asp Tyr Leu Ile Leu 865 870 875 880 Lys 431 2646 DNA Homo sapiens 431 atgcagcatc accaccatca ccacggagta cagcttcaag acaatgggta taatggattg 60 ctcattgcaa ttaatcctca ggtacctgag aatcagaacc tcatctcaaa cattaaggaa 120 atgataactg aagcttcatt ttacctattt aatgctacca agagaagagt atttttcaga 180 aatataaaga ttttaatacc tgccacatgg aaagctaata ataacagcaa aataaaacaa 240 gaatcatatg aaaaggcaaa tgtcatagtg actgactggt atggggcaca tggagatgat 300 ccatacaccc tacaatacag agggtgtgga aaagagggaa aatacattca tttcacacct 360 aatttcctac tgaatgataa cttaacagct ggctacggat cacgaggccg agtgtttgtc 420 catgaatggg cccacctccg ttggggtgtg ttcgatgagt ataacaatga caaacctttc 480 tacataaatg ggcaaaatca aattaaagtg acaaggtgtt catctgacat cacaggcatt 540 tttgtgtgtg aaaaaggtcc ttgcccccaa gaaaactgta ttattagtaa gctttttaaa 600 gaaggatgca cctttatcta caatagcacc caaaatgcaa ctgcatcaat aatgttcatg 660 caaagtttat cttctgtggt tgaattttgt aatgcaagta cccacaacca agaagcacca 720 aacctacaga accagatgtg cagcctcaga agtgcatggg atgtaatcac agactctgct 780 gactttcacc acagctttcc catgaacggg actgagcttc cacctcctcc cacattctcg 840 cttgtagagg ctggtgacaa agtggtctgt ttagtgctgg atgtgtccag caagatggca 900 gaggctgaca gactccttca actacaacaa gccgcagaat tttatttgat gcagattgtt 960 gaaattcata ccttcgtggg cattgccagt ttcgacagca aaggagagat cagagcccag 1020 ctacaccaaa ttaacagcaa tgatgatcga aagttgctgg tttcatatct gcccaccact 1080 gtatcagcta aaacagacat cagcatttgt tcagggctta agaaaggatt tgaggtggtt 1140 gaaaaactga atggaaaagc ttatggctct gtgatgatat tagtgaccag cggagatgat 1200 aagcttcttg gcaattgctt acccactgtg ctcagcagtg gttcaacaat tcactccatt 1260 gccctgggtt catctgcagc cccaaatctg gaggaattat cacgtcttac aggaggttta 1320 aagttctttg ttccagatat atcaaactcc aatagcatga ttgatgcttt cagtagaatt 1380 tcctctggaa ctggagacat tttccagcaa catattcagc ttgaaagtac aggtgaaaat 1440 gtcaaacctc accatcaatt gaaaaacaca gtgactgtgg ataatactgt gggcaacgac 1500 actatgtttc tagttacgtg gcaggccagt ggtcctcctg agattatatt atttgatcct 1560 gatggacgaa aatactacac aaataatttt atcaccaatc taacttttcg gacagctagt 1620 ctttggattc caggaacagc taagcctggg cactggactt acaccctgaa caatacccat 1680 cattctctgc aagccctgaa agtgacagtg acctctcgcg cctccaactc agctgtgccc 1740 ccagccactg tggaagcctt tgtggaaaga gacagcctcc attttcctca tcctgtgatg 1800 atttatgcca atgtgaaaca gggattttat cccattctta atgccactgt cactgccaca 1860 gttgagccag agactggaga tcctgttacg ctgagactcc ttgatgatgg agcaggtgct 1920 gatgttataa aaaatgatgg aatttactcg aggtattttt tctcctttgc tgcaaatggt 1980 agatatagct tgaaagtgca tgtcaatcac tctcccagca taagcacccc agcccactct 2040 attccaggga gtcatgctat gtatgtacca ggttacacag caaacggtaa tattcagatg 2100 aatgctccaa ggaaatcagt aggcagaaat gaggaggagc gaaagtgggg ctttagccga 2160 gtcagctcag gaggctcctt ttcagtgctg ggagttccag ctggccccca ccctgatgtg 2220 tttccaccat gcaaaattat tgacctggaa gctgtaaaag tagaagagga attgacccta 2280 tcttggacag cacctggaga agactttgat cagggccagg ctacaagcta tgaaataaga 2340 atgagtaaaa gtctacagaa tatccaagat gactttaaca atgctatttt agtaaataca 2400 tcaaagcgaa atcctcagca agctggcatc agggagatat ttacgttctc accccaaatt 2460 tccacgaatg gacctgaaca tcagccaaat ggagaaacac atgaaagcca cagaatttat 2520 gttgcaatac gagcaatgga taggaactcc ttacagtctg ctgtatctaa cattgcccag 2580 gcgcctctgt ttattccccc caattctgat cctgtacctg ccagagatta tcttatattg 2640 aaataa 2646 432 36 DNA Artificial Sequence Primer 432 cgcctgctcg agtcattaat attcatcaga aaatgg 36 433 371 PRT Homo sapiens 433 Met Gln His His His His His His Trp Gln Pro Leu Phe Phe Lys Trp 1 5 10 15 Leu Leu Ser Cys Cys Pro Gly Ser Ser Gln Ile Ala Ala Ala Ala Ser 20 25 30 Thr Gln Pro Glu Asp Asp Ile Asn Thr Gln Arg Lys Lys Ser Gln Glu 35 40 45 Lys Met Arg Glu Val Thr Asp Ser Pro Gly Arg Pro Arg Glu Leu Thr 50 55 60 Ile Pro Gln Thr Ser Ser His Gly Ala Asn Arg Phe Val Pro Lys Ser 65 70 75 80 Lys Ala Leu Glu Ala Val Lys Leu Ala Ile Glu Ala Gly Phe His His 85 90 95 Ile Asp Ser Ala His Val Tyr Asn Asn Glu Glu Gln Val Gly Leu Ala 100 105 110 Ile Arg Ser Lys Ile Ala Asp Gly Ser Val Lys Arg Glu Asp Ile Phe 115 120 125 Tyr Thr Ser Lys Leu Trp Ser Asn Ser His Arg Pro Glu Leu Val Arg 130 135 140 Pro Ala Leu Glu Arg Ser Leu Lys Asn Leu Gln Leu Asp Tyr Val Asp 145 150 155 160 Leu Tyr Leu Ile His Phe Pro Val Ser Val Lys Pro Gly Glu Glu Val 165 170 175 Ile Pro Lys Asp Glu Asn Gly Lys Ile Leu Phe Asp Thr Val Asp Leu 180 185 190 Cys Ala Thr Trp Glu Ala Met Glu Lys Cys Lys Asp Ala Gly Leu Ala 195 200 205 Lys Ser Ile Gly Val Ser Asn Phe Asn His Arg Leu Leu Glu Met Ile 210 215 220 Leu Asn Lys Pro Gly Leu Lys Tyr Lys Pro Val Cys Asn Gln Val Glu 225 230 235 240 Cys His Pro Tyr Phe Asn Gln Arg Lys Leu Leu Asp Phe Cys Lys Ser 245 250 255 Lys Asp Ile Val Leu Val Ala Tyr Ser Ala Leu Gly Ser His Arg Glu 260 265 270 Glu Pro Trp Val Asp Pro Asn Ser Pro Val Leu Leu Glu Asp Pro Val 275 280 285 Leu Cys Ala Leu Ala Lys Lys His Lys Arg Thr Pro Ala Leu Ile Ala 290 295 300 Leu Arg Tyr Gln Leu Gln Arg Gly Val Val Val Leu Ala Lys Ser Tyr 305 310 315 320 Asn Glu Gln Arg Ile Arg Gln Asn Val Gln Val Phe Glu Phe Gln Leu 325 330 335 Thr Ser Glu Glu Met Lys Ala Ile Asp Gly Leu Asn Arg Asn Val Arg 340 345 350 Tyr Leu Thr Leu Asp Ile Phe Ala Gly Pro Pro Asn Tyr Pro Phe Ser 355 360 365 Asp Glu Tyr 370 434 1119 DNA Homo sapiens 434 atgcagcatc accaccatca ccactggcag cccctcttct tcaagtggct cttgtcctgt 60 tgccctggga gttctcaaat tgctgcagca gcctccaccc agcctgagga tgacatcaat 120 acacagagga agaagagtca ggaaaagatg agagaagtta cagactctcc tgggcgaccc 180 cgagagctta ccattcctca gacttcttca catggtgcta acagatttgt tcctaaaagt 240 aaagctctag aggccgtcaa attggcaata gaagccgggt tccaccatat tgattctgca 300 catgtttaca ataatgagga gcaggttgga ctggccatcc gaagcaagat tgcagatggc 360 agtgtgaaga gagaagacat attctacact tcaaagcttt ggagcaattc ccatcgacca 420 gagttggtcc gaccagcctt ggaaaggtca ctgaaaaatc ttcaattgga ctatgttgac 480 ctctatctta ttcattttcc agtgtctgta aagccaggtg aggaagtgat cccaaaagat 540 gaaaatggaa aaatactatt tgacacagtg gatctctgtg ccacatggga ggccatggag 600 aagtgtaaag atgcaggatt ggccaagtcc atcggggtgt ccaacttcaa ccacaggctg 660 ctggagatga tcctcaacaa gccagggctc aagtacaagc ctgtctgcaa ccaggtggaa 720 tgtcatcctt acttcaacca gagaaaactg ctggatttct gcaagtcaaa agacattgtt 780 ctggttgcct atagtgctct gggatcccat cgagaagaac catgggtgga cccgaactcc 840 ccggtgctct tggaggaccc agtcctttgt gccttggcaa aaaagcacaa gcgaacccca 900 gccctgattg ccctgcgcta ccagctgcag cgtggggttg tggtcctggc caagagctac 960 aatgagcagc gcatcagaca gaacgtgcag gtgtttgaat tccagttgac ttcagaggag 1020 atgaaagcca tagatggcct aaacagaaat gtgcgatatt tgacccttga tatttttgct 1080 ggccccccta attatccatt ttctgatgaa tattaatga 1119 435 36 DNA Artificial Sequence Primer 435 ggatccgccg ccaccatgac atccattcga gctgta 36 436 27 DNA Artificial Sequence Primer 436 gtcgactcag ctggaccaca gccgcag 27 437 37 DNA Artificial Sequence Primer 437 ggatccgccg ccaccatgga ctcctggacc ttctgct 37 438 27 DNA Artificial Sequence Primer 438 gtcgactcag aaatcctttc tcttgac 27 439 933 DNA Homo sapiens 439 atggactcct ggaccttctg ctgtgtgtcc ctttgcatcc tggtagcaaa gcacacagat 60 gctggagtta tccagtcacc ccggcacgag gtgacagaga tgggacaaga agtgactctg 120 agatgtaaac caatttcagg acacgactac cttttctggt acagacagac catgatgcgg 180 ggactggagt tgctcattta ctttaacaac aacgttccga tagatgattc agggatgccc 240 gaggatcgat tctcagctaa gatgcctaat gcatcattct ccactctgaa gatccagccc 300 tcagaaccca gggactcagc tgtgtacttc tgtgccagca gtttagttgg agcaaacact 360 gaagctttct ttggacaagg caccagactc acagttgtag aggacctgaa caaggtgttc 420 ccacccgagg tcgctgtgtt tgagccatca gaagcagaga tctcccacac ccaaaaggcc 480 acactggtgt gcctggccac aggcttcttc cctgaccacg tggagctgag ctggtgggtg 540 aatgggaagg aggtgcacag tggggtcagc acggacccgc agcccctcaa ggagcagccc 600 gccctcaatg actccagata ctgcctgagc agccgcctga gggtctcggc caccttctgg 660 cagaaccccc gcaaccactt ccgctgtcaa gtccagttct acgggctctc ggagaatgac 720 gagtggaccc aggatagggc caaacccgtc acccagatcg tcagcgccga ggcctggggt 780 agagcagact gtggctttac ctcggtgtcc taccagcaag gggtcctgtc tgccaccatc 840 ctctatgaga tcctgctagg gaaggccacc ctgtatgctg tgctggtcag cgcccttgtg 900 ttgatggcca tggtcaagag aaaggatttc tga 933 440 822 DNA Homo sapiens 440 atgacatcca ttcgagctgt atttatattc ctgtggctgc agctggactt ggtgaatgga 60 gagaatgtgg agcagcatcc ttcaaccctg agtgtccagg agggagacag cgctgttatc 120 aagtgtactt attcagacag tgcctcaaac tacttccctt ggtataagca agaacttgga 180 aaaagacctc agcttattat agacattcgt tcaaatgtgg gcgaaaagaa agaccaacga 240 attgctgtta cattgaacaa gacagccaaa catttctccc tgcacatcac agagacccaa 300 cctgaagact cggctgtcta cttctgtgca gcaagtatac tgaacaccgg taaccagttc 360 tattttggga cagggacaag tttgacggtc attccaaata tccagaaccc tgaccctgcc 420 gtgtaccagc tgagagactc taaatccagt gacaagtctg tctgcctatt caccgatttt 480 gattctcaaa caaatgtgtc acaaagtaag gattctgatg tgtatatcac agacaaaact 540 gtgctagaca tgaggtctat ggacttcaag agcaacagtg ctgtggcctg gagcaacaaa 600 tctgactttg catgtgcaaa cgccttcaac aacagcatta ttccagaaga caccttcttc 660 cccagcccag aaagttcctg tgatgtcaag ctggtcgaga aaagctttga aacagatacg 720 aacctaaact ttcaaaacct gtcagtgatt gggttccgaa tcctcctcct gaaagtggcc 780 gggtttaatc tgctcatgac gctgcggctg tggtccagct ga 822 

1. An isolated polynucleotide comprising a sequence selected from the group consisting of: (a) sequences provided in SEQ ID NOs: 420, 424, 428, 431 and 434; (b) complements of the sequences provided in SEQ ID NOs: 370-375, 420, 424, 428, 431 and 434; (c) sequences consisting of at least 20 contiguous residues of a sequence provided in SEQ ID NOs:370-375, 420, 424, 428, 431 and 434; (d) sequences that hybridize to a sequence provided in SEQ ID NOs: 370-375, 420, 424, 428, 431 and 434, under moderately stringent conditions; (e) sequences having at least 75% identity to a sequence of SEQ ID NOs: 370-375, 420, 424, 428, 431 and 434; (f) sequences having at least 90% identity to a sequence of SEQ ID NOs: 370-375, 420, 424, 428, 431 and 434; and (g) degenerate variants of a sequence provided in SEQ ID NOs: 370-375, 420, 424, 428, 431 and
 434. 2. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of: (a) SEQ ID NOs: 423, 427, 430 and 433; (b) sequences encoded by a polynucleotide of claim 1; and (c) sequences having at least 70% identity to a sequence encoded by a polynucleotide of claim 1; and (d) sequences having at least 90% identity to a sequence encoded by a polynucleotide of claim
 1. 3. An expression vector comprising a polynucleotide of claim 1 operably linked to an expression control sequence.
 4. A host cell transformed or transfected with an expression vector according to claim
 3. 5. An isolated antibody, or antigen-binding fragment thereof, that specifically binds to a polypeptide of claim
 2. 6. A method for detecting the presence of a cancer in a patient, comprising the steps of: (a) obtaining a biological sample from the patient; (b) contacting the biological sample with a binding agent that binds to a polypeptide of claim 2; (c) detecting in the sample an amount of polypeptide that binds to the binding agent; and (d) comparing the amount of polypeptide to a predetermined cut-off value and therefrom determining the presence of a cancer in the patient.
 7. A fusion protein comprising at least one polypeptide according to claim
 2. 8. An oligonucleotide that hybridizes to a sequence recited in SEQ ID NOs: 370-375, 420, 424, 428, 431 and 434 under moderately stringent conditions.
 9. A method for stimulating and/or expanding T cells specific for a tumor protein, comprising contacting T cells with at least one component selected from the group consisting of: (a) polypeptides according to claim 2; (b) polynucleotides according to claim 1; and (c) antigen-presenting cells that express a polypeptide according to claim 2, under conditions and for a time sufficient to permit the stimulation and/or expansion of T cells.
 10. An isolated T cell population, comprising T cells prepared according to the method of claim
 9. 11. A composition comprising a first component selected from the group consisting of physiologically acceptable carriers and immunostimulants, and a second component selected from the group consisting of: (a) polypeptides according to claim 2; (b) polynucleotides according to claim 1; (c) antibodies according to claim 5; (d) fusion proteins according to claim 7; (e) T cell populations according to claim 10; and (f) antigen presenting cells that express a polypeptide according to claim
 2. 12. A method for stimulating an immune response in a patient, comprising administering to the patient a composition of claim
 11. 13. A method for the treatment of a cancer in a patient, comprising administering to the patient a composition of claim
 11. 14. A method for determining the presence of a cancer in a patient, comprising the steps of: (a) obtaining a biological sample from the patient; (b) contacting the biological sample with an oligonucleotide according to claim 8; (c) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide; and (d) compare the amount of polynucleotide that hybridizes to the oligonucleotide to a predetermined cut-off value, and therefrom determining the presence of the cancer in the patient.
 15. A diagnostic kit comprising at least one oligonucleotide according to claim
 8. 16. A diagnostic kit comprising at least one antibody according to claim 5 and a detection reagent, wherein the detection reagent comprises a reporter group.
 17. A method for inhibiting the development of a cancer in a patient, comprising the steps of: (a) incubating CD4+and/or CD8+T cells isolated from a patient with at least one component selected from the group consisting of: (i) polypeptides according to claim 2; (ii) polynucleotides according to claim 1; and (iii) antigen presenting cells that express a polypeptide of claim 2, such that T cell proliferate; (b) administering to the patient an effective amount of the proliferated T cells, and thereby inhibiting the development of a cancer in the patient.
 18. The fusion protein of claim 7, wherein the fusion protein comprises an amino acid sequence selected from the group consisting of: SEQ ID NOs:423, 427, 430 and
 433. 